Needle Guide Starter Kit

Reusable non-sterile bracket with Infiniti Plus™ (12, 14, 16, 18GA) needle guides (2), Infiniti Plus™ (18, 20, 21/22, 25GA) needle guides (3), (14 x 147cm) CIV-Flex™ covers (5) for use with…

Registry build 21.09.26

Reusable non-sterile bracket with Infiniti Plus™ (12, 14, 16, 18GA) needle guides (2), Infiniti Plus™ (18, 20, 21/22, 25GA) needle guides (3), (14 x 147cm) CIV-Flex™ covers (5) for use with FUJIFILM Sonosite HFL38, HFL38x, L38, L38e, and L38x transducers

44manufacturers in China registered for this device type
52catalogue numbers in this listing
15510(k) clearances naming this product code
28recalls on this code

Who Else Makes It

Concentrated in Guangdong (18), Jiangsu (10), Shanghai (3). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code ITX
Manufacturer City Province Registered as Device types
Jabil Circuit (Shanghai) Ltd. Shanghai Shanghai Contract manufacturer 31
Ming FAI Industrial (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 17
ATL Technology DG,Ltd. Dongguan Guangdong Contract manufacturer 14
Xuzhou Yongkang Electronic Science Technology Co., Ltd. Xuzhou Jiangsu Contract manufacturer 13
Hony Medical Co., Ltd. Taishan Guangdong Contract manufacturer 10
Xian Friendship Medical Electronics Co., Ltd. Xi’An Shaanxi Contract manufacturer 10
Taijia Medical Electronics (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 10
Chison Medical Technologies Co., Ltd. Wuxi Jiangsu Contract manufacturer 5
Philips Ultrasound (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 5
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56

Showing 12 of 44. All 44 manufacturers in China registered for Transducer, Ultrasonic, Diagnostic

Record

Regulatory record for Needle Guide Starter Kit
Listed by Civco Medical Instruments Co., Inc., United States
FDA product code ITX
Device type Transducer, Ultrasonic, Diagnostic
Device class Class 2
Regulation 21 CFR 892.1570
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K093713
Record published 2022-11-22
Record revised 2022-06-10 (version 10)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Keep Away from Sunlight
Sizes Length 1.78 to 13.5 in; width 0.9 to 1.6 in; height 1.15 to 2.07 in; length 14 cm; width 147 cm
Distribution end date 2021-08-20

Catalogue Numbers

Catalogue numbers for Needle Guide Starter Kit
Catalogue number Size Status
671-003 In distribution
P27068-01 In distribution
674-031-T Length 3.2 in In distribution
674-044 Length 13.5 in In distribution
674-038 Length 1.8 in In distribution
P01882-08 Width 1.58 in In distribution
11654277 In distribution
671-002 Length 14 cm In distribution
P12051-02 Width 1.25 in In distribution
P28643-01 In distribution
P27062-01 In distribution
P28639-01 In distribution
P07873-02 Length 1.99 in In distribution
687-003 In distribution
P18710-01 Height 1.89 in In distribution
674-070 In distribution
P28662-01 In distribution
P28773-01 In distribution
P28775-01 In distribution
674-037 Length 1.8 in In distribution
P12868-03 Height 1.9 in In distribution
P28642-01 In distribution
P12920-03 Width 1.17 in In distribution
674-059 Length 2.8 in In distribution
674-052 Length 3.8 in In distribution
P22244-01 Length 1.98 in In distribution
674-030-T Length 2.4 in In distribution
P01300-08 Length 3.76 in In distribution
693-013 In distribution
674-061 Length 3.9 in In distribution
674-039 Length 1.8 in In distribution
P28664-01 In distribution
P05187-04 Width 1.22 in In distribution
P04999-04 Width 1.49 in In distribution
P27060-01 In distribution
P18708-01 Length 2.85 in In distribution
P27064-01 In distribution
693-011 In distribution
P15679-01 Length 3.91 in In distribution
680-186 In distribution
674-030 Height 1.2 in In distribution
674-036 Length 3.69 in In distribution
P27066-01 In distribution
674-035 Height 1.2 in In distribution
674-031 Height 1.3 in In distribution
P28645-01 In distribution
687-001 In distribution
P12868-02 Height 1.9 in Withdrawn
P12922-02 Width 1.17 in Withdrawn
P12920-02 Width 1.17 in Withdrawn
674-072 Width 1.5 in Withdrawn
P12924-02 Width 1.17 in Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
SonoScape Sonoscape Medical Corp. 302
Biopsy Starter Kit Civco Medical Instruments Co., Inc. 172
Sheathes Sheathing Technologies, Inc. 170
Needle Guide Civco Medical Instruments Co., Inc. 156
Sheathes3D Sheathing Technologies, Inc. 78
Ultrasound Probe Cover Biopsy Needle Guide Advance Medical Designs, Inc. 78
ultrasonic transducer Edan Instruments, Inc. 70
Unbranded Advance Medical Designs, Inc. 68
Reusable Biopsy Bracket Protek Medical Products, Inc. 60
Ultrasound Probe Cover Biopsy Needle Guide Kit Advance Medical Designs, Inc. 58
Biopsy Bracket Civco Medical Instruments Co., Inc. 56
Transducer Cover Civco Medical Instruments Co., Inc. 54

Showing 12 of 1,678. All products under Transducer, Ultrasonic, Diagnostic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K231783 2023-11-14
K222052 2022-11-22
K211270 2021-09-13
K163313 2017-06-09
K160806 2016-08-05
K131161 2013-09-17
K131528 2013-06-11
K093713 2010-01-19
K013721 2001-12-28
K992152 1999-08-17
K991236 1999-06-02
K970513 1997-06-20
K970514 1997-06-20
K970515 1997-06-20
K843573 1984-12-13

Recalls Naming This Product

23 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Needle Guide Starter Kit
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Civco Medical Instruments Co., Inc. 510(k) number 2025-05-01 Class II Process design During the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle guide can cause a pinhole breach in the transducer cover when latching the guide in place. 506 boxes
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly. 738 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly. 1,375 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly. 948 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other 73 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other 297 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other 115 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other 257 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other 234 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other 66 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other 468 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other 613 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other 20 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other 49 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other 3 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-11-02 Class II Other 135 boxes 2020-11-20
Civco Medical Instruments Co., Inc. 510(k) number 2018-02-23 Class II Device Design A cover failed leak testing during validation testing of new needle guides from a replacement tool. 177 boxes 2020-10-06
Civco Medical Instruments Co., Inc. 510(k) number 2015-10-21 Class II Process design Sterility of the product cannot be assured. 717 boxes 2017-02-28
Civco Medical Instruments Co., Inc. 510(k) number 2015-10-21 Class II Process design Sterility of the product cannot be assured. 508 boxes 2017-02-28
Civco Medical Instruments Co., Inc. 510(k) number 2015-10-21 Class II Process design Sterility of the product cannot be assured. 1139 boxes 2017-02-28
Civco Medical Instruments Co., Inc. 510(k) number 2015-10-21 Class II Process design Sterility of the product cannot be assured. 206 boxes 2017-02-28
Civco Medical Instruments Co., Inc. 510(k) number 2015-10-21 Class II Process design Sterility of the product cannot be assured. 54 boxes 2017-02-28
Fujifilm Sonosite,inc. 510(k) number 2005-12-12 Not classified Other 22 gauge needle guides were intermixed with 21 gauge guides and labeled as 21 gauge needle guides. 355 boxes/24 kits per box 2006-07-31

Recalls

3 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2018-07-30 Class II Process control The assembly of the needle guides were found to be either missing adhesive or did not have adequate adhesive to hold the assembled cannula in place on the needle guide. 3 units 2020-09-16
2018-07-30 Class II Process control The assembly of the needle guides were found to be either missing adhesive or did not have adequate adhesive to hold the assembled cannula in place on the needle guide. 107 units 2020-09-16
2015-02-26 Class II Process design Leaks were detected in the recalled lot which may compromise the sterility of the product. 120 pouches 2017-02-28
2011-01-21 Not classified Labeling design Non-sterile transducer covers were incorrectly labeled as sterile and contained incorrect temperature storage information. 31/24-cover boxes 2013-07-09
2010-07-20 Not classified Nonconforming Material/Component Polyethylene material did not have proper treatment applied during manufacturing. Untreated polyethylene material does not maintain a secure seal with the adhesive tape used to secure the tip to the cover. 22 boxes 2012-04-13
2008-01-16 Not classified Packaging Incorrect Needle Guide- The individual pouches contained V53W Endocavity Needle guide(p/n/034-054) instead of the Shimadzu T/R Needle guide (p/n134-054). Lot M102250 – 5 boxes; Lot M105440 – 2 boxes 2008-04-03

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