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G7 Mini Tray 110002765

by Biomet Orthopedics, Inc.

G7 Mini Tray 110002765 is a Class II device made by Biomet Orthopedics, Inc., listed in FDA GUDID since 19 Oct 2018 (UDI-DI 00880304566507), 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 Number00880304566507 UDI-DI Date19 Oct 2018ListedStatusListed 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  • Withdrawn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
G7 Mini Tray
Generic name
Joint prosthesis implantation kit, reusable
Model / Ref / Catalog
110002765
Primary DI / UDI-DI
00880304566507
FDA product code
OQG, OQI, PBI, LZO, LPH, JDI, OQH, KWZ
GMDN term
Joint prosthesis implantation kit, reusable
Device class
Class II
Regulation number
888.3358, 888.3353, 888.3310, 888.3350
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Joint prosthesis implantation kit, reusable

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Other devices filed under Joint prosthesis implantation kit, reusable.

Other devices from Biomet Orthopedics, Inc.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)