Skip to content

Avenue L IR90017R

by Ldr Spine USA

Avenue L IR90017R is a tendon/ligament graft preparation station (FDA Class I; FDA product code LXH, Orthopedic Manual Surgical Instrument) made by Ldr Spine USA, listed in FDA GUDID since 13 Dec 2018 (UDI-DI 03662663039604), 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 Number03662663039604 UDI-DI Date13 Dec 2018ListedStatusListed 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  • Withdrawn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
Avenue L
Generic name
Tendon/ligament graft preparation station
Model / Ref / Catalog
IR90017R
Primary DI / UDI-DI
03662663039604
FDA product code
LXH
GMDN term
Tendon/ligament graft preparation station
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Tendon/ligament graft preparation station

Similar devices in this category

Other devices filed under Tendon/ligament graft preparation station.

Other devices from Ldr Spine USA

See all devices from Ldr Spine USA →

Properties

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