Skip to content

ProAM ALIF System LN-014229-1214

by Pro Surgical, Inc.

ProAM ALIF System LN-014229-1214 is a Class I device made by Pro Surgical, Inc., listed in FDA GUDID since 24 Jan 2025 (UDI-DI 00810152902356), 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 Number00810152902356 UDI-DI Date24 Jan 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  • Withdrawn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
ProAM ALIF System
Generic name
Spinal implant trial
Model / Ref / Catalog
LN-014229-1214
Primary DI / UDI-DI
00810152902356
FDA product code
LXH
GMDN term
Spinal implant trial
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Spinal implant trial

Other devices from Pro Surgical, Inc.

See all devices from Pro Surgical, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)