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Invictus CI-10132-13

by Alphatec Spine, Inc.

Invictus CI-10132-13 is a Class I device made by Alphatec Spine, Inc., listed in FDA GUDID since 19 Sep 2020 (UDI-DI 00811801031588), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00811801031588 UDI-DI Date19 Sep 2020ListedStatusListed 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  • Withdrawn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
Invictus
Generic name
Bone distraction forceps
Model / reference
CI-10132-13
Primary DI / UDI-DI
00811801031588
FDA product code
HTD
GMDN term
Bone distraction forceps
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone distraction forceps

Similar devices in this category

Other devices filed under Bone distraction forceps.

Other devices from Alphatec Spine, Inc.

See all devices from Alphatec Spine, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)