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Cmp-00536

by Integrity Implants Inc.

Ref CMP-00536

Cmp-00536 is a Class I device made by Integrity Implants Inc., registered in EUDAMED on 10 Jun 2022 (Basic UDI-DI B-00810004727182) and listed in FDA GUDID since 10 Mar 2020 (UDI-DI 00810004727182), active as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00810004727182 Basic UDI-DI 00810004727182UDI-DIDate10 Jun 2022RegisteredStatusActive
United StatesGUDID listing GUDID Number00810004727182 UDI-DI Date10 Mar 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00810004727182 registered 10 Jun 2022 Active
  • FDA GUDID UDI-DI 00810004727182 listed 10 Mar 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00810004727182
  2. Registered EUDAMED B-00810004727182

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
FlareHawk Interbody Fusion System
Generic name
Orthopaedic surgical distractor, internal
Model / Ref / Catalog
CMP-00536
Primary DI / UDI-DI
00810004727182
Basic UDI-DI
B-00810004727182
FDA product code
LXH
EMDN code
L0920 Orthopaedic surgery distractors, reusable
GMDN term
Orthopaedic surgical distractor, internal
Device class
Class I
Regulation number
888.4540
EU registration type
Legacy device (under a directive)
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic surgical distractor, internal

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY DISTRACTORS, REUSABLE.

Other devices from Integrity Implants Inc.

See all devices from Integrity Implants Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (18, all answered No)