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GreenLight XPS 0010-0210

by American Medical Systems, Inc.

GreenLight XPS 0010-0210 is a Class II device made by American Medical Systems, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00878953005508), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00878953005508 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
GreenLight XPS
Generic name
General/multiple surgical frequency-doubled solid-state laser system
Model / reference
0010-0210
Primary DI / UDI-DI
00878953005508
FDA product code
GEX
GMDN term
General/multiple surgical frequency-doubled solid-state laser system
Device class
Class II
Regulation number
878.4810
GUDID distribution status
In Commercial Distribution

Related devices

Category: General/multiple surgical frequency-doubled solid-state laser system

Similar devices

Other devices filed under FDA product code GEX (Powered Laser Surgical Instrument).

Other devices from American Medical Systems, Inc.

See all devices from American Medical Systems, Inc. →

Properties

  • Prescription use
  • Lot / batch number
  • Serial number
Other properties (12, all answered No)