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Invictus 16142

by Alphatec Spine, Inc.

Invictus 16142 is a Class I device made by Alphatec Spine, Inc., listed in FDA GUDID since 17 Jun 2020 (UDI-DI 00190376148663), 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 Number00190376148663 UDI-DI Date17 Jun 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  • Withdrawn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
Orthopaedic implant/instrument assembling device
Model / reference
16142
Primary DI / UDI-DI
00190376148663
FDA product code
LXH
GMDN term
Orthopaedic implant/instrument assembling device
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic implant/instrument assembling device

Similar devices in this category

Other devices filed under Orthopaedic implant/instrument assembling device.

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)