Tlx 5800019

by NuVasive, LLC

Tlx 5800019 is a Class I device made by NuVasive, LLC, listed in FDA GUDID since 24 Sep 2018 (UDI-DI 00887517729484), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00887517729484 UDI-DI	Date24 Sep 2018Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00887517729484

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Tlx
Generic name: Orthopaedic implant/instrument dismantling device
Model / reference: 5800019

Primary DI / UDI-DI: 00887517729484
FDA product code: LXH
GMDN term: Orthopaedic implant/instrument dismantling device

Device class: Class I
Regulation number: 888.4540
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number

Other properties (11, all answered No)