BD Luer-Lok

Syringe Blunt Fill 5ML LL W/NDL 18X1-1/2

Registry build 21.09.26
60manufacturers in China registered for this device type
50catalogue numbers in this listing
14510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (16), Zhejiang (15), Shanghai (11). 12 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FMF
Manufacturer City Province Registered as Device types
Jiangsu Caina Medical Co., Ltd. Jiangyin Jiangsu Contract manufacturer 20
BQ Plus Medical Co., Ltd. Songjiang Shanghai Contract manufacturer 13
Medwell Technology Limited Dongguan Guangdong Contract manufacturer 10
Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd. Chengdu Sichuan Contract manufacturer 10
Zhejiang Runqiang Medical Instruments Co., Ltd. Jiaxing Zhejiang Contract manufacturer 9
Wuxi Yushou Medical Appliances Co., Ltd. Wuxi Jiangsu Contract manufacturer 8
Pine Moon Electronics Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Shenzhen HYS Medical Co., Ltd. Shenzhen Guangdong Contract manufacturer 6
Yangzhou Xingwei Medical Technology Co., Ltd. Yangzhou Jiangsu Contract manufacturer 5
Zhejiang INI Medical Devices Co., Ltd. Wenzhou Zhejiang Contract manufacturer 4
ShanDong WeiGao Group Medical Polymer Co., Ltd. Weihai Shandong Contract manufacturer 3
Hantech (Ningbo) Medical Technology Co., Ltd. Ningbo Zhejiang Contract manufacturer 3

Showing 12 of 60. All 60 manufacturers in China registered for Syringe, Piston

Record

Regulatory record for BD Luer-Lok
Listed by Becton, Dickinson AND Company, United States
FDA product code FMF
Device type Syringe, Piston
Device class Class 2
Regulation 21 CFR 880.5860
Establishment Contract manufacturer, Contract steriliser, Specification developer, Repacker / relabeller, Manufacturer
510(k) K110771
Record published 2016-09-19
Record revised 2025-08-07 (version 8)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Over the counter Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Keep away from sunlight; Special storage condition: Keep dry
Packaging Pack or inner pack of 100, case of 8, case of 4, case of 12, pack or inner pack of 10, pack or inner pack of 40
Sizes Total volume 1 to 50 ml; needle gauge 18 to 26 G; length 0.625 to 1.5 in
Distribution end date 2023-03-29
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for BD Luer-Lok
Catalogue number Size Per pack Status
309588 Needle Gauge 23 G In distribution
309589 Total Volume 3 ml In distribution
309657 200 In distribution
309635 Length 1.5 in In distribution
309582 Total Volume 3 ml In distribution
309653 Total Volume 50 ml In distribution
309644 Length 1 in In distribution
309680 In distribution
309643 Length 1.5 in In distribution
309632 Length 1 in In distribution
309577 100 In distribution
303310 Total Volume 20 ml In distribution
309570 Total Volume 3 ml In distribution
309599 Length 1.5 in In distribution
309585 100 In distribution
309628 Total Volume 1 ml In distribution
309571 Needle Gauge 23 G In distribution
309574 100 In distribution
309633 Length 1.5 in In distribution
309695 Total Volume 10 ml In distribution
309702 25 In distribution
309580 Needle Gauge 18 G In distribution
305617 In distribution
309587 Length 0.625 in In distribution
305618 In distribution
309645 Length 1.5 in In distribution
305062 Total Volume 5 ml In distribution
309604 100 In distribution
309630 Length 1 in In distribution
309637 Needle Gauge 20 G In distribution
309569 Total Volume 3 ml In distribution
309646 125 In distribution
305060 Needle Gauge 18 G In distribution
309598 Length 1 in In distribution
309572 Total Volume 3 ml In distribution
309605 20 In distribution
309640 Length 1 in In distribution
309581 Length 1 in In distribution
309631 Total Volume 5 ml In distribution
309703 25 In distribution
309579 100 In distribution
301604 Total Volume 10 ml In distribution
305064 Needle Gauge 18 G In distribution
309578 100 In distribution
309642 Length 1 in In distribution
309634 Total Volume 5 ml In distribution
309575 100 In distribution
309661 40 Withdrawn
309629 100 Withdrawn
309650 40 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Yeso med Wuxi Yushou Medical Appliances Co., Ltd. 228
Medallion® Merit Medical Systems, Inc. 223
Merit Medical® Merit Medical Systems, Inc. 192
Monoject Cardinal Health 188
Medline Medline Industries, Inc. 127
EasyTouch MHC Medical Products 122
Medline Industries, Inc. Medline Industries, Inc. 99
Arrow Teleflex Medical LLC 94
Ceros Rhino Medical Supply Inc 92
Enteral Feeding Medela LLC 87
Monoject Cardinal Health 200, LLC 83
HSW Soft-Ject® Henke-Sass Wolf, Gmbh. 80

Showing 12 of 913. All products under Syringe, Piston

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K251350 2025-07-29
K212499 2022-03-09
K203359 2021-07-28
K203453 2021-01-25
K201234 2020-07-15
K190054 2019-10-21
K182589 2019-03-14
K172670 2018-10-23
K162081 2016-12-19
K151870 2016-07-08
K151766 2015-09-02
K121283 2012-05-30
K110771 2011-05-13
K010890 2001-04-19

Recalls Naming This Product

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

Recalls naming the identifiers of BD Luer-Lok
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Mentor Texas LP 510(k) number 2026-04-28 Class II Process control A single lot of expired syringes were distributed due to a distribution system control failure. 1401 syringes
Becton, Dickinson & Co. 510(k) number 2016-09-16 Class II Process control BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required. 22,400 units 2018-03-20
Becton, Dickinson & Co. 510(k) number 2016-09-16 Class II Process control BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required. 57600 units 2018-03-20
Becton, Dickinson & Co. 510(k) number 2016-09-16 Class II Process control BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required. 340,000 units 2018-03-20
Becton, Dickinson & Co. 510(k) number 2016-09-16 Class II Process control BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required of 10-6. 648,000 units 2018-03-20
Becton, Dickinson & Co. 510(k) number 2016-09-16 Class II Process control BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required. 547,600 units 2018-03-20
Becton, Dickinson & Co. 510(k) number 2016-09-16 Class II Process control BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required. 1,528,000 units 2018-03-20
Becton, Dickinson & Co. 510(k) number 2016-03-25 Class II Error in labeling BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm x 25 mm) and Henry Schein 10 mL Single Use Syringe Luer-Lock are being recalled due to possible adulteration and non-conforming manufacturing practices. 176,000 units 2017-04-03
Becton, Dickinson & Co. 510(k) number 2016-03-25 Class II Error in labeling BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm x 25 mm) and Henry Schein 10 mL Single Use Syringe Luer-Lock are being recalled due to possible adulteration and non-conforming manufacturing practices. 811,200 units 2017-04-03
Becton, Dickinson & Co. 510(k) number 2014-12-19 Class II Device Design The stopper of the 10mL BD Luer-Lok syringe is not properly seated in the syringe. 564,000 units 2015-12-07

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