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General Instruments CI-11539

by Alphatec Spine, Inc.

General Instruments CI-11539 is a Class I device made by Alphatec Spine, Inc., listed in FDA GUDID since 2 Jun 2024 (UDI-DI 00840180526712), 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 Number00840180526712 UDI-DI Date2 Jun 2024ListedStatusListed 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  • Withdrawn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
Operating table orthopaedic extension, non-powered
Model / reference
CI-11539
Primary DI / UDI-DI
00840180526712
FDA product code
CCX
GMDN term
Operating table orthopaedic extension, non-powered
Device class
Class I
Regulation number
868.6820
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Operating table orthopaedic extension, non-powered

Similar devices in this category

Other devices filed under Operating table orthopaedic extension, non-powered.

Other devices from Alphatec Spine, Inc.

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Properties

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