CRANIOFIX2

Craniofix 2 Titanium Clamp 16MM

Registry build 21.09.26
3manufacturers in China registered for this device type
3catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (2), 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 GXN
Manufacturer City Province Registered as Device types
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
B.Braun Medical (Suzhou) Co,.Ltd Suzhou Jiangsu Contract manufacturer 37
Kontour (Xi’an) Medical Technology Co., Ltd. Xi’An Shaanxi Contract manufacturer 4

Record

Regulatory record for CRANIOFIX2
Listed by Aesculap AG, Germany
FDA product code GXN
Device type Plate, Cranioplasty, Preformed, Non-Alterable
Device class Class 2
Regulation 21 CFR 882.5330
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2015-09-24
Record revised 2025-06-09 (version 8)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for CRANIOFIX2
Catalogue number Size Per pack Status
FF491T 6 In distribution
FF490T 12 In distribution
FF492T 6 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
HTR-Pekk Oxford Performance Materials, Inc. 4,551
Kelyniam CSI Kelyniam Global Inc. 1,714
Plate, Cranioplasty, Preformed, Non-Alterable Synthes Gmbh 263
PEEK Patient Specific Cranial/Craniofacial Implant(PSCI) Kontour (Xi’an) Medical Technology Co., Ltd. 162
CranioFit Bioplate, Inc. 161
IPS KLS-Martin L.P. 74
AccuShape MedCAD 27
ClearFit Longeviti Neuro Solutions 26
IPS, Sterile KLS-Martin L.P. 18
Level ONE Thoracic, Sterile KLS-Martin L.P. 14
Meticuly Patient-specific titanium mesh implant Meticuly Co., Ltd. 13
Bioplate® Bioplate, Inc. 13

Showing 12 of 32. All products under Plate, Cranioplasty, Preformed, Non-Alterable

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K122353 2012-08-30
K040864 2004-06-17
K972332 1998-01-16

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