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Tregor® 200095

by Aston Medical

Tregor® 200095 (12561970U) is a Class II device made by Aston Medical, listed in FDA GUDID since 16 Sep 2015 (UDI-DI 03663703000097), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03663703000097 UDI-DI Date16 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Tregor®
Generic name
Acetabular shell
Model / Ref / Catalog
200095, 12561970U
Primary DI / UDI-DI
03663703000097
FDA product code
MEH
GMDN term
Acetabular shell
Device class
Class II
Regulation number
888.3353
GUDID distribution status
In Commercial Distribution

Related devices

Category: Acetabular shell

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Other devices filed under Acetabular shell.

Other devices from Aston Medical

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)