Medline

Vantex 7FR 3L 20CM CVC Stock + Bundle US

Registry build 21.09.26
24manufacturers in China registered for this device type
1,960catalogue numbers in this listing
5510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (11), Anhui (6), Zhejiang (4). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LRO
Manufacturer City Province Registered as Device types
Conod Medical Co., Limited Changshu Jiangsu Contract manufacturer 48
Principle & Will Biotech (Pinghu) Co., Ltd. Pinghu Zhejiang Contract manufacturer 39
Sino Protection (Hefei) Medical Products Co., Ltd. Hefei Anhui Contract manufacturer 18
Changzhou Holymed Products Co., Ltd. Changzhou Jiangsu Contract manufacturer 16
Donghai Xingchen NON-Woven Products Co., Ltd. North Donghai Development Zone, Lianyungang Jiangsu Contract manufacturer 7
Fengyang Jiehong Nonwoven Product Co., Ltd. Chuzhou Anhui Contract manufacturer 7
3A Medical Products Co., Ltd. Liu An Anhui Contract manufacturer 6
Cobes Industries (Jinzhai) Co., Ltd. Luan Anhui Contract manufacturer 6
Lianyungang Aiyeh Non-woven Products Co., Ltd. Lianyungang Jiangsu Contract manufacturer 6
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Ningbo Greetmed Medical Instruments Co., Ltd. Ningbo Zhejiang Specification developer 75
GRI Medical & Electronic Technology Co., Ltd. Jiaxing Zhejiang Contract manufacturer 71

Showing 12 of 24. All 24 manufacturers in China registered for General Surgery Tray

Record

Regulatory record for Medline
Listed by Medline Industries, Inc., United States
FDA product code LRO
Device type General Surgery Tray
Device class Class 2
Regulation 21 CFR 878.4370
510(k) K213481
Record published 2024-07-03
Record revised 2025-07-15 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Over the counter Yes
Supplied as a kit Yes
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date, manufacturing date, serial number
Storage Special storage condition: Avoid contact with an open flame or high intensity heat source
Packaging Case of 5, case of 20, case of 10, case of 50, case of 6
Distribution end date 2026-01-29
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Medline
Catalogue number Size Status
STCVC01USGV In distribution
ECVC6915A In distribution
DYNJ902965A In distribution
DYNJ0368098P In distribution
DYNDH1406 In distribution
DYNDH1355A In distribution
CMPV85204LBPA In distribution
EBSI1342 In distribution
ECVC8385B In distribution
PICC0019 In distribution
DYNDC2079 In distribution
DYNDA2755 In distribution
DYNDH1983A In distribution
DYNDV2617 In distribution
ECVC2065 In distribution
DYNDB3007A In distribution
DYKM1034 In distribution
ECVC8611 In distribution
EBSI1514 In distribution
DYNDC2399A In distribution
STCVCNC01 In distribution
ECVC4575 In distribution
DYNJP8240S In distribution
ECVC1180A In distribution
DYNJP1065A In distribution
STCVC01US In distribution
DYNJ0689066B In distribution
CMPV85162LBA In distribution
SPEC0196B In distribution
DYNJ0792596B In distribution
P171237 In distribution
ECVC8490 In distribution
ARTNC204 In distribution
DYNJ902631A In distribution
P972300A In distribution
STCVC02USGV In distribution
I550BF85NL In distribution
ECVC2290B In distribution
DYNJ0368008P In distribution
ECVC3505 In distribution
EBSI1282 In distribution
DYNDA2431 In distribution
PICCFI4155 In distribution
PICC0020 In distribution
LC460 In distribution
DYNJP9150A In distribution
DYNDL1847 In distribution
DYNJ0782855 In distribution
ECVC8652 In distribution
DYNDV2556 In distribution
P588892 In distribution
DYKM1027 In distribution
DYKD100EPKLF1 In distribution
MIDST0019 In distribution
ACC010431 In distribution
DYNDL1602 In distribution
EBSI1221A In distribution
DYKM1088 In distribution
ECVC150A In distribution
DYNDC3417A In distribution
SPEC0254A In distribution
I301BF85 In distribution
DYNJ0781615AG In distribution
DYNJ0990957K In distribution
DYNDC1461G In distribution
ECVC2500 In distribution
CVI4905 In distribution
ECVC6975 In distribution
DYNDB3020 In distribution
DYKM1095 In distribution
ECVC6550A In distribution
DYNDL1550 In distribution
ECVC7200A In distribution
ECVC8597 In distribution
ECVC8627 In distribution
DYNJ0389010N In distribution
DYNDH1271A In distribution
MIDF4120 In distribution
ECVC8651 In distribution
DYNDL1596A In distribution
CVI4810 In distribution
DYNDL1425B In distribution
ECVC8045 In distribution
PICCB5255 In distribution
DYNJP3030A In distribution
ECVC2595 In distribution
DYNDA2669 In distribution
DYNDB3038 In distribution
ECVC4545 In distribution
MID0001 In distribution
DYNJ0392184J In distribution
MIDB4120 In distribution
DYNDL1517 In distribution
DYNDC3427 In distribution
DYNDH1532 In distribution
STCVC85162BPA In distribution
ECVC4105 In distribution
STCVC2055US In distribution
DYNDH1223A In distribution
PICCFI6360 In distribution
EBSI1207A In distribution
ECVC4300 In distribution
PACG1104 In distribution
MNS11605A In distribution
PICC0013 In distribution
DYNJP8010 In distribution
ECVC8475 In distribution
EBSI1533A In distribution
DYNDV2359 In distribution
DYNDC1986 In distribution
BSIPIV1005A In distribution
ECVC8240 In distribution
PICC2620MB In distribution
ECVC6555A In distribution
DYNDC3403 In distribution
EBSI1645 In distribution
DYNDL1470 In distribution
STCVC01145B In distribution
DYNJ902628B In distribution
DYKE1172 In distribution
DYNJ0826390S In distribution
ECVC7205B In distribution
DYKM1096 In distribution
PICC0020 In distribution
EBSI1081 In distribution
STCVC41US In distribution
DYNDB3006A In distribution
ECVC8649 In distribution
ECVC1835 In distribution
IVS4222A In distribution
ECVC3755A In distribution
DYNDL1723 In distribution
DYNDB3041 In distribution
P737057 In distribution
EBSI1489 In distribution
DYNDL1796 In distribution
DYNJP9100 In distribution
DYNDL1687 In distribution
CVI5338 In distribution
ECVC5640A In distribution
DT23065 In distribution
ECVC8055 In distribution
EBSI1231C In distribution
EBSI1881A In distribution
DYNJ0149530D In distribution
ECVC6395 In distribution
DYNJ0392216K In distribution
ECVC8255 In distribution
DYNDH1420 In distribution
DYNDC3437 In distribution
DYK200MRSA In distribution
DYNDA1126 In distribution
ECVC2675 In distribution
DYNJP8110 In distribution
DYNDH1480 In distribution
DYKM1940 In distribution
DYNJP3000UG In distribution
DYNJP5020SI In distribution
ECVC5055 In distribution
CMPCVI85BC In distribution
DYNDL1050 In distribution
DYNDL1399 In distribution
DYNJP1035 In distribution
ECVC1500 In distribution
DYNDH1293B In distribution
MID0007A In distribution
DYNDC1940 In distribution
ECVC7355 In distribution
DYNJ39657C In distribution
DYNJ0303039G In distribution
DYNJ53339A In distribution
DYNDH1176 In distribution
DYNDB3037 In distribution
EBSI1136B In distribution
ECVC2670A In distribution
ECVC8355 In distribution
A5028VF09 In distribution
ECVC7000 In distribution
DYNDH1328 In distribution
DYNDL1954 In distribution
DYNJP7010 In distribution
ECVC8105 In distribution
ECVC4985 In distribution
DYNDL1770B In distribution
ECVC8560 In distribution
DYNJP8441 In distribution
ECVC5020A In distribution
ECVC8285 In distribution
ECVC7605 In distribution
ECVC6590 In distribution
EBSI1537A In distribution
ECVC6680A In distribution
ECVC7660 In distribution
DYNDB3009 In distribution
EBSI1739 In distribution
DYKM2698A In distribution
SPEC0291B In distribution
CMPM7203LBB In distribution
ART1280A In distribution
ECVC7070B In distribution
ECVC2940 In distribution
DYNDC2605 In distribution
ECVC8634 In distribution
EBSI1779A In distribution
STCVC21US In distribution
DYNDV2567 In distribution
DYNJ904057 In distribution
ECVC360 In distribution
ECVC7460 In distribution
EBSI1780 In distribution
ECVC6840 In distribution
DYNJP3100 In distribution
DYNDL1312A In distribution
CVI5195 In distribution
ECVC1185A In distribution
DYNDL1616 In distribution
DYNDC2951C In distribution
CDS980246U In distribution
DYNDH2199 In distribution
ECVC5260 In distribution
ART1185B In distribution
EBSI1690 In distribution
CDS860040J In distribution
DYNDA2469 In distribution
ECVC6985B In distribution
ECVC8425A In distribution
ECVC3165 In distribution
DYNDC3085A In distribution
ECVC8616 In distribution
DYNJ0751263M In distribution
DYNDC2225 In distribution
STCVC01UST In distribution
CDS983034M In distribution
EBSI1688 In distribution
PICCB4260 In distribution
DYNDV2547C In distribution
DYNJP1055A In distribution
DYNJ0778413B In distribution
CVI4655A In distribution
DYNDC2410B In distribution
DYNJ54867 In distribution
ECVC3470 In distribution
DT5490B In distribution
ECVC7495B In distribution
ECVC290 In distribution
DYNJ0737856G In distribution
DYK1006300I In distribution
P392929 In distribution
ECVC7630 In distribution
DYNDL1314 In distribution

Showing 250 of 300 catalogue numbers.

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Cardinal Health Cardinal Health 200, LLC 67,931
Medline Industries, Inc. Medline Industries, Inc. 54,362
Avid TruCustom Avid Medical, Inc. 13,498
Halyard Avid Medical, Inc. 12,802
ACS American Contract Systems, Inc. 10,337
SurgiTrack Owens & Minor Distribution, Inc. 5,575
Aligned Medical Solutions Aligned Medical Solutions 3,490
SurgiTrackSM Owens & Minor Distribution, Inc. 3,364
DeRoyal Deroyal Industries, Inc. 2,770
Henry Schein Henry Schein, Inc. 729
Stradis Stradis Healthcare 685
Centurion Centurion Medical Products Corporation 672

Showing 12 of 113. All products under General Surgery Tray

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K213481 2022-05-24
K212258 2021-12-03
K970286 1997-03-10
K962826 1996-09-16
K930700 1993-07-09

Recalls Naming This Product

55 recalls name this product by its own identifiers, the UDI on its label or the 510(k) it is cleared under.

Recalls naming the identifiers of Medline
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Medline Industries, LP – Northfield 510(k) number 2026-07-31 Not classified Under Investigation by firm Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used. 60
Medline Industries, LP – Northfield 510(k) number 2026-07-23 Not classified Packaging process control The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach. Sterility of the product cannot be assured. If a compromised pouch seal is not identified prior to use and the cannu 135 units
Medline Industries, LP – Northfield 510(k) number 2026-07-20 Class II Nonconforming Material/Component Downstream recall – manufacturer recalled specific lots of BD ChloraPrep Clear – 1mL Applicators. Affected product may exhibit an open or incomplete seal on the packaging of the applicator. Use of potentially contaminated applicator may lea 222,653 total
Medline Industries, LP – Northfield 510(k) number 2026-07-10 Class II Process change control Kits contain a potentially contaminated component which were recalled by the manufacturer 663 kits
Medline Industries, LP – Northfield 510(k) number 2026-07-08 Class II Nonconforming Material/Component Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of endotoxin of the neurosponges. 246 kits
Medline Industries, LP – Northfield 510(k) number 2026-06-12 Class II Nonconforming Material/Component The kits contain BD ChloraPrep Clear – 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding which may extend to the seal area. If the sterile barrier is co 434,595 kits
Medline Industries, LP – Northfield 510(k) number 2026-06-10 Class II Under Investigation by firm Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health consequences from use of product include clinically insignificant extension of surgery to f 163 kits
Medline Industries, LP – Northfield 510(k) number 2026-06-08 Class I Nonconforming Material/Component The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to quality issues that could result in drug ineffectiveness. 52 kits
Medline Industries, LP – Northfield 510(k) number 2026-06-05 Class I Under Investigation by firm Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose Injection, USP. B. Braun Medical Inc. was notified by their supplier, Spectra Medic 60 kits
Medline Industries, LP – Northfield 510(k) number 2026-05-28 Class II Process change control Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen d 9,272 kits
Medline Industries, LP – Northfield 510(k) number 2026-05-28 Class II Under Investigation by firm Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in i 396 kits
Medline Industries, LP – Northfield 510(k) number 2026-05-21 Class II Nonconforming Material/Component The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing in 48075 kits
Medline Industries, LP – Northfield 510(k) number 2026-05-04 Class II Nonconforming Material/Component During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached pr 123030 units
Medline Industries, LP – Northfield 510(k) number 2026-04-27 Class II Process control Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application. 49,654 kits total
Medline Industries, LP – Northfield 510(k) number 2026-04-27 Class II Process control Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application. 49,654 kits total
Medline Industries, LP – Northfield 510(k) number 2026-04-27 Class II Process control Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application. 49,654 kits total
Medline Industries, LP – Northfield 510(k) number 2026-04-10 Class I Component design/selection Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complai 30120 kits
Medline Industries, LP – Northfield 510(k) number 2026-03-16 Class II Under Investigation by firm On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile. 640 kits
Medline Industries, LP – Northfield 510(k) number 2026-03-16 Class II Under Investigation by firm Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the 40845 kits
Medline Industries, LP – Northfield 510(k) number 2026-02-27 Class II Component change control Unapproved design changes to the products outside of the 510(k) clearance. 270,311 total
Medline Industries, LP – Northfield 510(k) number 2026-02-27 Class II No Marketing Application Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA.
Products not initially reported in RES 98601.
113,843 kits
Medline Industries, LP – Northfield 510(k) number 2026-02-16 Class II Under Investigation by firm Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragmen 14,379 kits total
Medline Industries, LP – Northfield UDI-DI 2026-01-08 Class II Process control Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the 14,525
Medline Industries, LP – Northfield 510(k) number 2026-01-08 Class II Process control Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the 1212
Medline Industries, LP – Northfield UDI-DI 2026-01-07 Class II Under Investigation by firm Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have 154427 units
Medline Industries, LP – Northfield UDI-DI 2026-01-07 Class II Under Investigation by firm Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have 14,927,765 units
Medline Industries, LP – Northfield UDI-DI 2026-01-07 Class II Under Investigation by firm Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have 193157 units
Medline Industries, LP – Northfield 510(k) number 2026-01-07 Class II Process control Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have 207196 units
Medline Industries, LP – Northfield UDI-DI 2026-01-07 Class II Process control Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have 14927765 units
Medline Industries, LP – Northfield UDI-DI 2026-01-07 Class II Process control Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have 193157 units
Medline Industries, LP – Northfield 510(k) number 2025-12-24 Class II Packaging change control Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators. 21854 units
Medline Industries, LP – Northfield UDI-DI 2025-12-12 Class II Nonconforming Material/Component Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive. 857 units
Medline Industries, LP – Northfield 510(k) number 2025-10-10 Class I Nonconforming Material/Component Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120″ expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may resu 96,406 total units
Medline Industries, LP – Northfield 510(k) number 2025-09-10 Class II Process control Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking. 950 units
Medline Industries, LP – Northfield 510(k) number 2025-08-08 Class I Process control Convenience kits labeled as sterile have not gone through the sterilization process. 22 units
Medline Industries, LP – Northfield 510(k) number 2025-07-08 Class II Unknown/Undetermined by firm Affected kits contain recalled Stryker Color Cuff Sterile Disposable Tourniquet Cuffs. Stryker Instruments initiated this recall due to a potential manufacturing defect in which the flange may detach from the bladder at the welded connectio 1145
Medline Industries, LP – Northfield 510(k) number 2025-04-22 Class I Nonconforming Material/Component Affected kits contain recalled Integra Lifesciences Codman Disposable Perforators due to inadequate welds on specific lots. Perforators with inadequate welds may break or separate. 1853 total
Medline Industries, LP – Northfield 510(k) number 2025-02-24 Class I Process change control Specific Medline Kits were manufactured using Intubation ORAL/NASAL Endotracheal Tubes which were subsequently recalled by Smiths Medical. 1550 units
Medline Industries, LP – Northfield UDI-DI 2025-02-13 Class II Packaging process control Potential breach in pouch packaging which could lead to loss of sterility. 1,490 units
Medline Industries, LP – Northfield 510(k) number 2025-02-13 Class II Packaging process control Potential breach in pouch packaging which could lead to loss of sterility. 2,422 units

Showing 40 of 55.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer