DRLock™

Proximal Non-Locking Screw

Registry build 21.09.26
22manufacturers in China registered for this device type
46catalogue numbers in this listing
4510(k) clearances naming this product code
5recalls on this code

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (4), Zhejiang (3). 12 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HRS
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Kingj Medical Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Hangzhou Sino-MIM Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Suzhou AND Science & Technology Development Corp. Zhangjiagang Jiangsu Contract manufacturer 5
Beijing AK Medical Co., Ltd. Changping District Beijing Contract manufacturer 3

Showing 12 of 22. All 22 manufacturers in China registered for Plate, Fixation, Bone

Record

Regulatory record for DRLock™
Listed by Tornier Inc., United States
FDA product code HRS
Device type Plate, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2015-10-16
Record revised 2025-11-20 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number
Sizes Outer diameter 2 to 2.4 mm; length 10 to 14 mm
Distribution end date 2022-11-01

Catalogue Numbers

Catalogue numbers for DRLock™
Catalogue number Size Status
DRV-002-1L Withdrawn
DRV-011-35-16 Withdrawn
DRV-121-20-14 Withdrawn
DRV-121-20-24 Withdrawn
DRV-011-24-14 Outer Diameter 2.4 mm Withdrawn
DRV-011-24-22 Withdrawn
DRV-021-24-14 Withdrawn
DRV-021-24-16 Withdrawn
DRV-021-35-08 Withdrawn
DRV-002-0L Withdrawn
DRV-021-24-18 Withdrawn
DRV-002-4R Withdrawn
DRV-002-4L Withdrawn
DRV-002-0R Size Short Withdrawn
DRV-121-20-18 Withdrawn
DRV-021-24-26 Withdrawn
DRV-121-20-28 Withdrawn
DRV-121-20-26 Withdrawn
DRV-011-35-10 Withdrawn
DRV-021-24-12 Withdrawn
DRV-011-24-16 Withdrawn
DRV-011-35-14 Withdrawn
DRV-021-35-18 Withdrawn
DRV-011-24-18 Withdrawn
DRV-001-4L Withdrawn
DRV-121-20-22 Withdrawn
DRV-021-24-24 Withdrawn
DRV-021-24-28 Withdrawn
DRV-021-24-22 Withdrawn
DRV-021-24-20 Withdrawn
DRV-121-20-20 Withdrawn
DRV-021-35-10 Withdrawn
DRV-011-35-18 Withdrawn
DRV-121-20-16 Withdrawn
DRV-121-20-10 Length 10 mm Withdrawn
DRV-021-35-16 Withdrawn
DRV-021-24-10 Withdrawn
DRV-001-1R Withdrawn
DRV-011-24-20 Withdrawn
DRV-121-20-12 Withdrawn
DRV-021-35-12 Withdrawn
DRV-002-1R Withdrawn
DRV-001-4R Withdrawn
DRV-021-35-14 Withdrawn
DRV-011-35-12 Withdrawn
DRV-001-1L Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pectus System Biomet Microfixation 4,662
Arthrex® Arthrex, Inc. 3,031
Evos Smith & Nephew, Inc. 2,235
Peri-Loc Smith & Nephew, Inc. 2,196
OsteoMed Osteomed 1,961
VariAx Stryker GmbH 1,934
Aptus Medartis Inc. 1,688
TC-100 Smith & Nephew, Inc. 1,639
Plate, Fixation, Bone Synthes Gmbh 1,613
Anthem Globus Medical, Inc. 1,551
Acumed Acumed LLC 1,360
Signex Osteonic Co., Ltd. 1,310

Showing 12 of 3,530. All products under Plate, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K191711 2019-07-17
K181587 2018-10-05
K090139 2009-10-27
K090582 2009-07-02

Recalls

The FDA has not published a severity grade for these. 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
2011-08-22 Not classified Nonconforming Material/Component The firm discovered a testing protocol error, in both dynamic and static cantilever comparative testing, during the initial comparative testing. 2,722 units 2012-02-19
2011-07-06 Not classified Nonconforming Material/Component The surgical tray does not meet our Instruction for Use (IFU) for dry time requirement. 61 trays 2012-09-10
2007-09-04 Not classified Component change control Seat/Fit problems: The heads of the distal screws/pegs rest above the surface of the distal plate after the screws/pegs are fully tightened. 267 plates/52 DRL System Trays 2011-05-20
2006-08-03 Not classified Other The 48 distal locking-screws (ranging from 10-24mm) contained in the kit are not within established specifications, specifically the minor diameter of the screws are undersized. 180 2012-09-10
2005-11-01 Not classified Other Screwdriver pilot taper tip can break during surgery. 14 2012-04-25

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