Tregor® 33347

by Aston Medical

Tregor® 33347 (12522870) is a Class II device made by Aston Medical, listed in FDA GUDID since 16 Sep 2015 (UDI-DI 03663703000004), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number03663703000004 UDI-DI	Date16 Sep 2015Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 03663703000004

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Tregor®
Generic name: Constrained polyethylene acetabular liner
Model / Ref / Catalog: 33347, 12522870

Primary DI / UDI-DI: 03663703000004
FDA product code: LZO
GMDN term: Constrained polyethylene acetabular liner

Device class: Class II
Regulation number: 888.3353
GUDID distribution status: In Commercial Distribution

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Other devices filed under Constrained polyethylene acetabular liner.

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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)