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Aston Medical

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Aston Medical is a medical device manufacturer, with 112 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 12 Nov 2026.

Devices
112

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 109
  • FDA 510(k) 3

A device listed in two registries counts in both.

Device classes
  • FDA Class II 112
Identifiers
  • DUNS 576503098

What Aston Medical makes

Aston Medical manufactures orthopedic implants for hip and shoulder arthroplasty, including acetabular shells, polyethylene acetabular liners, shoulder prosthesis stems, and reverse shoulder prostheses. Their product line includes uncoated and coated shoulder humeral stems, reverse shoulder prosthesis bodies and base plates, and specialized components like constrained polyethylene liners for hip replacements.

The company’s devices are classified as Class II under FDA regulations and are authorised through 510(k) clearances and the FDA’s Unique Device Identification (UDI) system. These products are listed in the FDA’s regulatory databases and are intended for use in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue112

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Company details

DUNS number
576503098
Phone
+33477930004

Frequently asked questions

How many devices does Aston Medical have in the registry?

The registry currently lists 112 devices for Aston Medical. Devices recorded under merged duplicate company entries are counted once.

Which registries list Aston Medical's devices?

Among its 50 most recently registered devices, Aston Medical has devices listed in FDA GUDID (50 devices).

What risk classes do Aston Medical's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Aston Medical's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Aston Medical in the registry?

The most recently registered devices listed for Aston Medical include Duocentric® 50430, TREGOR® 36515STER, TREGOR® 37060 and Duocentric® 50390.

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