Quikflap

2 Hole PLATES(3) Self Drilling SCREW(6)

Registry build 21.09.26
3manufacturers in China registered for this device type
3catalogue numbers in this listing
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (1), Shanghai (1), Shaanxi (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JEY
Manufacturer City Province Registered as Device types
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Kontour (Xi’an) Medical Technology Co., Ltd. Xi’An Shaanxi Contract manufacturer 4

Record

Regulatory record for Quikflap
Listed by Stryker Leibinger Gmbh & Co. KG, Germany
FDA product code JEY
Device type Plate, Bone
Device class Class 2
Regulation 21 CFR 872.4760
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
510(k) K862482
Record published 2015-09-24
Record revised 2025-06-09 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Distribution end date 2023-07-13

Catalogue Numbers

Catalogue numbers for Quikflap
Catalogue number Size Status
12-01500 In distribution
12-01100 In distribution
12-01110 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Plate, Bone Stryker Leibinger Gmbh & Co. KG 1,338
Level ONE CMF KLS-Martin L.P. 1,160
Medicon Medicon eG. Chirurgiemechaniker-Genossenschaft 843
OsteoMed Osteomed 675
Bioplate® Bioplate, Inc. 669
Plate, Bone Synthes Gmbh 568
Leforte System Bone Plate Jeil Medical Corporation 466
CMF Visionare Visionare LLC 421
Level ONE CMF, Sterile KLS-Martin L.P. 416
Faico CMF System Faico Medical, LLC 361
TraumaOne System Biomet Microfixation 357
MatrixMANDIBLE Synthes Gmbh 277

Showing 12 of 152. All products under Plate, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K240651 2024-07-12
K230733 2023-08-05
K221855 2022-11-09
K000594 2000-12-08

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