Skip to content

Avanta Orthopaedics, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
18
FDA recalls
1

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Avanta Orthopaedics, Inc. makes

Avanta Orthopaedics, Inc. makes orthopaedic implants and fixation devices for the hand and upper extremity, including trapeziometacarpal joint implants such as the Trapezial and Trapezium Implants, radial head implants, finger joint prostheses, tendon spacers, and external fixation systems like the K'Fix and Scaphix staple fixation devices.

The company's devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; Avanta Orthopaedics, Inc. is based in the United States.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue18

Newest first, rows 1-18 of 18

Search and filter all 18 devices
Skip device list

Rows 1-18 of 18

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

  • 2003

    • 24 Jan 2003 Z-0710-03 Unclassified (pre-2012) Terminated Wrong silicone elastomer used in construction. Distribution: States of CA and UT and to France. Submission number: K964381

Frequently asked questions

How many devices does Avanta Orthopaedics, Inc. have in the registry?

The registry currently lists 18 devices for Avanta Orthopaedics, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Avanta Orthopaedics, Inc.'s devices?

Among its 18 most recently registered devices, Avanta Orthopaedics, Inc. has devices listed in FDA 510(k) (18 devices).

What risk classes do Avanta Orthopaedics, Inc.'s devices fall under?

Among its 18 most recently registered devices, the classes recorded for Avanta Orthopaedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Avanta Orthopaedics, Inc.?

FDA recall records list 1 recall initiated by Avanta Orthopaedics, Inc., the most recent initiated on 2003-01-24. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Avanta Orthopaedics, Inc. in the registry?

The most recently registered devices listed for Avanta Orthopaedics, Inc. include AVANTA ORTHOPAEDICS TRAPEZIAL IMPLANT, K'FIX, EXTERNAL FIXATION and AVANTA ORTHOPAEDICS TRAPEZIUM IMPLANT.

Generated automatically from registry data and not verified by a human reviewer.