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GMReis Suture Anchors

by Gm Dos Reis Industria E Comercio Ltda 28 variants

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 Number07899258601816 UDI-DI Date10 Dec 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Tendon/ligament bone anchor, non-bioabsorbable
Model / Ref / Catalog
PRESSLOCK - IMPACTED KNOTLESS PEEK ANCHOR Ø2.9x7.5/12.5mm WITH CLOSED EYELET, 320-29125
Primary DI / UDI-DI
07899258601816
FDA Product Code
MBI
GMDN Term
Tendon/ligament bone anchor, non-bioabsorbable
Device Class
Class II
Regulation Number
888.3040
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Other devices from Gm Dos Reis Industria E Comercio Ltda

See all devices from Gm Dos Reis Industria E Comercio Ltda →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No