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General Instruments CI-10776

by Alphatec Spine, Inc.

General Instruments CI-10776 is a Class I device made by Alphatec Spine, Inc., listed in FDA GUDID since 6 Aug 2021 (UDI-DI 00840180504093), 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 Number00840180504093 UDI-DI Date6 Aug 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  • Withdrawn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

Trade name
General Instruments
Generic name
Abdominal/ENT/orthopaedic surgical probe, reusable
Model / reference
CI-10776
Primary DI / UDI-DI
00840180504093
FDA product code
HXB
GMDN term
Abdominal/ENT/orthopaedic surgical probe, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Abdominal/ENT/orthopaedic surgical probe, reusable

Similar devices in this category

Other devices filed under Abdominal/ENT/orthopaedic surgical probe, 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)