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General Instrument CI-10941

by Alphatec Spine, Inc.

General Instrument CI-10941 is a Class I device made by Alphatec Spine, Inc., listed in FDA GUDID since 13 Oct 2022 (UDI-DI 00840180507995), 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 Number00840180507995 UDI-DI Date13 Oct 2022ListedStatusListed 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  • Withdrawn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
General Instrument
Generic name
Surgical depth gauge, single-use
Model / reference
CI-10941
Primary DI / UDI-DI
00840180507995
FDA product code
HTJ
GMDN term
Surgical depth gauge, single-use
Device class
Class I
Regulation number
888.4300
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical depth gauge, single-use

Similar devices in this category

Other devices filed under Surgical depth gauge, single-use.

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)