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IdentiTi CI-10383-16

by Alphatec Spine, Inc.

IdentiTi CI-10383-16 is a Class I device made by Alphatec Spine, Inc., listed in FDA GUDID since 19 Sep 2020 (UDI-DI 00811801038167), 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 Number00811801038167 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  • Withdrawn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
IdentiTi
Generic name
Bone lever/elevator, reusable
Model / reference
CI-10383-16
Primary DI / UDI-DI
00811801038167
FDA product code
HTE
GMDN term
Bone lever/elevator, reusable
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 lever/elevator, reusable

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)