SupraFuser B Generator

Ultrasonic Generator replacement for Generator BoneWelder 150-W1

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

All of them in Shanghai.

Chinese manufacturers registered for FDA product code MAI
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Arthrex (Shanghai) Co., Ltd. Shanghai Shanghai Exporter 38

Record

Regulatory record for SupraFuser B Generator
Listed by Surgical Fusion Technologies GmbH, Switzerland
FDA product code MAI
Device type Fastener, Fixation, Biodegradable, Soft Tissue
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K171228
Record published 2024-02-06
Record revised 2024-11-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Handling environment atmospheric pressure 70 to 106 KiloPascal; Handling environment humidity 30 to 75 % RH; Storage environment atmospheric pressure 50 to 106 KiloPascal; Storage environment humidity 10 to 85 % RH; Handling environment temperature 50 to 86 °F; Storage environment temperature 14 to 122 °F
Distribution end date 2024-11-28

Catalogue Numbers

Catalogue numbers for SupraFuser B Generator
Catalogue number Size Status
SupraFuser B Generator Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arthrex® Arthrex, Inc. 545
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Delta Stryker Leibinger Gmbh & Co. KG 110
Reunite Screw System Biomet Orthopedics 85
ComposiTCP S.B.M 61
ActivaScrew™ Interference Bioretec Ltd. 54
Ligafix S.B.M 40
Twinfix Smith & Nephew, Inc. 28
Biosure Smith & Nephew, Inc. 27
TorqLoc Interference Bioretec Ltd. 27
FiberFIX Nanova BIO Materials Inc 25
AlphaVent Stryker GmbH 23

Showing 12 of 176. All products under Fastener, Fixation, Biodegradable, Soft Tissue

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K260294 2026-03-27
K240288 2024-04-01

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