SmartLock

Dorsal Radius Fract.pl,locking,ri,medium

Registry build 21.09.26
22manufacturers in China registered for this device type
60catalogue numbers in this listing
25510(k) clearances naming this product code
1recall

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 SmartLock
Listed by Stryker GmbH, Switzerland
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
Record published 2015-09-24
Record revised 2025-04-14 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Sizes Length 10 to 28 mm
Distribution end date 2022-07-29

Catalogue Numbers

Catalogue numbers for SmartLock
Catalogue number Size Per pack Status
54-25277S Number of Screw Holes: 10.0 Holes Withdrawn
54-25286 Number of Screw Holes: 10.0 Holes Withdrawn
52-27314S Length 14.0 mm Withdrawn
52-27320E Length 20.0 mm Withdrawn
54-25284 Number of Screw Holes: 10.0 Holes Withdrawn
54-25277 Number of Screw Holes: 10.0 Holes Withdrawn
52-27324S Length 24.0 mm Withdrawn
52-27318E Length 18.0 mm Withdrawn
52-27314E Diameter: 2.7 Millimeter Withdrawn
52-27328S Diameter: 2.7 Millimeter Withdrawn
54-25288S Number of Screw Holes: 8.0 Holes Withdrawn
52-27326S Diameter: 2.7 Millimeter Withdrawn
54-25279 Number of Screw Holes: 10.0 Holes Withdrawn
52-27316E Diameter: 2.7 Millimeter Withdrawn
52-27310 Length 10.0 mm 5 Withdrawn
54-25280S Number of Screw Holes: 10.0 Holes Withdrawn
54-25289S Number of Screw Holes: 10.0 Holes Withdrawn
52-27316 Length 16.0 mm 5 Withdrawn
54-25283S Number of Screw Holes: 12.0 Holes Withdrawn
54-25284S Number of Screw Holes: 10.0 Holes Withdrawn
52-27318S Diameter: 2.7 Millimeter Withdrawn
52-27326E Diameter: 2.7 Millimeter Withdrawn
54-25281 Number of Screw Holes: 12.0 Holes Withdrawn
54-25287S Number of Screw Holes: 10.0 Holes Withdrawn
52-27310E Length 10.0 mm Withdrawn
52-27312E Diameter: 2.7 Millimeter Withdrawn
54-25289 Number of Screw Holes: 10.0 Holes Withdrawn
52-27320 Length 20.0 mm 5 Withdrawn
52-27318 Length 18.0 mm 5 Withdrawn
52-27324E Length 24.0 mm Withdrawn
54-25278S Number of Screw Holes: 10.0 Holes Withdrawn
52-27328E Diameter: 2.7 Millimeter Withdrawn
54-25286S Number of Screw Holes: 10.0 Holes Withdrawn
52-27322E Length 22.0 mm Withdrawn
52-27316S Diameter: 2.7 Millimeter Withdrawn
52-27312 Diameter: 2.7 Millimeter 5 Withdrawn
52-27322S Diameter: 2.7 Millimeter Withdrawn
54-25282 Number of Screw Holes: 10.0 Holes Withdrawn
52-27312S Diameter: 2.7 Millimeter Withdrawn
52-27326 Diameter: 2.7 Millimeter 5 Withdrawn
52-27322 Diameter: 2.7 Millimeter 5 Withdrawn
54-25283 Number of Screw Holes: 12.0 Holes Withdrawn
54-25280 Number of Screw Holes: 10.0 Holes Withdrawn
54-25285 Number of Screw Holes: 10.0 Holes Withdrawn
54-25281S Number of Screw Holes: 12.0 Holes Withdrawn
92-25278 Number of Screw Holes: 9.0 Holes Withdrawn
52-27320S Diameter: 2.7 Millimeter Withdrawn
52-27328 Length 28.0 mm 5 Withdrawn
54-25285S Number of Screw Holes: 10.0 Holes Withdrawn
54-25288 Number of Screw Holes: 8.0 Holes Withdrawn
92-25276 Number of Screw Holes: 9.0 Holes Withdrawn
54-25287 Number of Screw Holes: 10.0 Holes Withdrawn
52-27324 Length 24.0 mm 5 Withdrawn
54-25279S Number of Screw Holes: 10.0 Holes Withdrawn
54-25282S Number of Screw Holes: 10.0 Holes Withdrawn
52-27310S Diameter: 2.7 Millimeter Withdrawn
54-25276 Number of Screw Holes: 10.0 Holes Withdrawn
52-27314 Diameter: 2.7 Millimeter 5 Withdrawn
54-25276S Number of Screw Holes: 10.0 Holes Withdrawn
54-25278 Number of Screw Holes: 10.0 Holes 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
K242445 2024-10-06
K233919 2024-03-25
K231257 2023-08-18
K231262 2023-08-18
K222381 2023-04-27
K223772 2023-04-07
K221346 2022-07-08
K212581 2022-01-19
K200398 2020-06-05
K192675 2019-11-22
K191412 2019-08-23
K183172 2019-03-05
K181091 2018-10-11
K172148 2018-03-19
K172350 2017-12-15
K170727 2017-06-22
K170771 2017-05-08
K162841 2017-02-21
K162439 2017-02-03
K153379 2016-05-26
K151769 2015-10-27
K151879 2015-08-06
K113109 2011-12-23
K112926 2011-12-19
K110476 2011-03-18

Recalls

1 of these is 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
2019-12-05 Class II Under Investigation by firm Instrument can break at the level of the thread when being exposed to high forces during nail implantation or removal which can lead to complications during nail insertion and removal. 433 (289 units U.S. / 144 units OUS) 2020-10-09

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