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Ingenix 55057555

by Ingenium Spine

Ingenix 55057555 is a Class II device made by Ingenium Spine, listed in FDA GUDID since 24 Feb 2025 (UDI-DI 00843672101831), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00843672101831 UDI-DI Date24 Feb 2025ListedStatusListed 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  • Withdrawn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
Ingenix
Generic name
Spinal bone screw, non-bioabsorbable
Model / reference
55057555
Primary DI / UDI-DI
00843672101831
FDA product code
KNB
GMDN term
Spinal bone screw, non-bioabsorbable
Device class
Class II
Regulation number
884.4500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Spinal bone screw, non-bioabsorbable

Similar devices in this category

Other devices filed under Spinal bone screw, non-bioabsorbable.

Other devices from Ingenium Spine

  • Ingenix 55056535

    Class II

  • Ingenix 55017570

    Class II

  • Ingenix 60015545

    Class II

  • Ingenix 55016540

    Class II

See all devices from Ingenium Spine →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (6, all answered No)