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TROCAR 4.0mm 0608

by Advanced Orthopaedic Solutions, Inc.

TROCAR 4.0mm 0608 is a Class I device made by Advanced Orthopaedic Solutions, Inc., listed in FDA GUDID since 24 Feb 2016 (UDI-DI 00848665002393), 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 Number00848665002393 UDI-DI Date24 Feb 2016ListedStatusListed 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  • Withdrawn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
TROCAR 4.0mm
Generic name
Orthopaedic trocar blade, reusable
Model / reference
0608
Primary DI / UDI-DI
00848665002393
FDA product code
LXH
GMDN term
Orthopaedic trocar blade, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic trocar blade, reusable

Other devices from Advanced Orthopaedic Solutions, Inc.

See all devices from Advanced Orthopaedic Solutions, Inc. →

Properties

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