LessRay 8230013

by NuVasive, LLC

LessRay 8230013 is a Class II device made by NuVasive, LLC, listed in FDA GUDID since 4 Apr 2017 (UDI-DI 00887517756725), 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	Number00887517756725 UDI-DI	Date4 Apr 2017Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00887517756725

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: LessRay
Generic name: Diagnostic x-ray digital imaging system workstation
Model / reference: 8230013

Primary DI / UDI-DI: 00887517756725
FDA product code: JAA, LLZ, OWB
GMDN term: Diagnostic x-ray digital imaging system workstation

Device class: Class II
Regulation number: 892.1650, 892.2050
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use
Lot / batch number

Other properties (12, all answered No)