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RETRA Single - GEN 2 Depricated 5500-RB

by A.M. Surgical, 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 Number10857915007030 UDI-DI Date4 Jun 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  • Withdrawn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
RETRA Single - GEN 2 Depricated
Generic Name
Arthroscopic surgical procedure kit, non-medicated, single-use
Model / Reference
5500-RB
Primary DI / UDI-DI
10857915007030
FDA Product Code
NBH
GMDN Term
Arthroscopic surgical procedure kit, non-medicated, single-use
Device Class
Class I
Regulation Number
888.1100
GUDID distribution status
In Commercial Distribution

Other devices from A.M. Surgical, Inc.

See all devices from A.M. Surgical, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No