Techfit

Patient Match Cranial Implant, Medium, 55-100 cm^2 PEEK

Registry build 21.09.26
2manufacturers in China registered for this device type
6catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (1), Shanghai (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GWO
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

Record

Regulatory record for Techfit
Listed by Techfit Digital Surgery, Inc., United States
FDA product code GWO
Device type Plate, Cranioplasty, Preformed, Alterable
Device class Class 2
Regulation 21 CFR 882.5320
510(k) K250297
Record published 2025-12-30
Record revised 2026-04-03 (version 2)

Specifications

Specifications
MRI safety MR Safe
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number, manufacturing date, serial number
Distribution end date 2026-04-02

Catalogue Numbers

Catalogue numbers for Techfit
Catalogue number Size Status
0 Withdrawn
0 Withdrawn
0 Withdrawn
0 Withdrawn
0 Withdrawn
0 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
OsteoMed Osteomed 103
Plate, Cranioplasty, Preformed, Alterable Stryker Leibinger Gmbh & Co. KG 93
1.5MM System Biomet Microfixation 72
Customized Skull Implant (CSI) Kelyniam Global Inc. 49
Universal Neuro 3 Stryker Leibinger Gmbh & Co. KG 35
2.0MM System Biomet Microfixation 26
Resorb XG, Sterile KLS-Martin L.P. 26
Plate, Cranioplasty, Preformed, Alterable Biomet Microfixation 22
Innovasis® Cranial System Inno-Health Technology Co., Ltd. 21
NeuroPro® Low Profile Kinamed, Inc. 16
Leforte Neuro System Bone Plate Jeil Medical Corporation 14
Neuro & Craniofacial Fixation System Inno-Health Technology Co., Ltd. 11

Showing 12 of 45. All products under Plate, Cranioplasty, Preformed, Alterable

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K250297 2025-10-27

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