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Avenger M07S0011

by Medartis Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07630894827723 UDI-DI Date13 Oct 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Avenger
Generic Name
Orthopaedic prosthesis implantation positioning instrument, single-use
Model / Ref / Catalog
M07S0011
Primary DI / UDI-DI
07630894827723
FDA Product Code
LXH
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, single-use
Device Class
Class I
Regulation Number
888.4540
GUDID distribution status
In Commercial Distribution

Other devices from Medartis Inc.

See all devices from Medartis Inc. →

Properties

  • Sterile
  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No