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Invictus 17810

by Alphatec Spine, Inc.

Invictus 17810 is a Class I device made by Alphatec Spine, Inc., listed in FDA GUDID since 5 Dec 2021 (UDI-DI 00190376331720), 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 Number00190376331720 UDI-DI Date5 Dec 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  • Withdrawn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
Invictus
Generic name
Surgical apron, single-use
Model / reference
17810
Primary DI / UDI-DI
00190376331720
FDA product code
KTZ
GMDN term
Surgical apron, single-use
Device class
Class I
Regulation number
888.4150
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical apron, single-use

Similar devices

Also classified as Surgical apron, single-use.

Similar devices

Other devices filed under FDA product code KTZ (CALIPER).

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)