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Comprehensive Reverse Shoulder 180507

by Biomet Orthopedics, Inc.

Comprehensive Reverse Shoulder 180507 is a Class II device made by Biomet Orthopedics, Inc., listed in FDA GUDID since 24 Oct 2015 (UDI-DI 00880304475472), 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 Number00880304475472 UDI-DI Date24 Oct 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  • Withdrawn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
Comprehensive Reverse Shoulder
Generic name
Shoulder prosthesis screw
Model / Ref / Catalog
180507
Primary DI / UDI-DI
00880304475472
FDA product code
PAO, HSD, MBF, KWT, KWS
GMDN term
Shoulder prosthesis screw
Device class
Class II
Regulation number
888.3660, 888.3690, 888.3670, 888.3650
GUDID distribution status
In Commercial Distribution

Related devices

Category: Shoulder prosthesis screw

Similar devices in this category

Other devices filed under Shoulder prosthesis screw.

Other devices from Biomet Orthopedics, Inc.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)