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Cmp-02154

by Integrity Implants Inc.

Cmp-02154 is a Class I device made by Integrity Implants Inc., listed in FDA GUDID since 17 Nov 2021 (UDI-DI 00840200405539), 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 Number00840200405539 UDI-DI Date17 Nov 2021ListedStatusListed 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  • Withdrawn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

Generic name
Spinal guidewire
Model / Ref / Catalog
CMP-02154
Primary DI / UDI-DI
00840200405539
FDA product code
HXI
GMDN term
Spinal guidewire
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Spinal guidewire

Similar devices

Other devices filed under FDA product code HXI (Passer, Wire, Orthopedic).

Other devices from Integrity Implants Inc.

See all devices from Integrity Implants Inc. →

Properties

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