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LightLas SeLecTor Deux

by Lightmed Corporation 3 variants

Ref ST0023Model LightLas SeLecTor Deux

LightLas SeLecTor Deux (ST0023) is a device classified as Class IIb in the EU and Class II in the US made by Lightmed Corporation, registered in EUDAMED on 29 Apr 2025 (Basic UDI-DI B-04712826770956), cleared under FDA 510(k) K090774 on 13 Aug 2009 and listed in FDA GUDID since 8 Apr 2020 (UDI-DI 04712826770956), active as of 25 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDD 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 25 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K090774

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04712826770956 Basic UDI-DI 04712826770956UDI-DIDate29 Apr 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04712826770956 UDI-DI Date8 Apr 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k) GUDID from GUDID NumberK090774 Date13 Aug 2009IssuedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-04712826770956 registered 29 Apr 2025 Active
  • FDA 510(k) K090774 decided 13 Aug 2009 Active
  • FDA GUDID UDI-DI 04712826770956 listed 8 Apr 2020 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K090774
  2. Listed FDA GUDID 04712826770956
  3. Registered EUDAMED B-04712826770956

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Generic name
General/multiple surgical frequency-doubled solid-state laser system
Device name
Ophthalmic YAG Laser System and Accessories
Model / reference
LightLas SeLecTor Deux, ST0023
Primary DI / UDI-DI
04712826770956
Basic UDI-DI
B-04712826770956
510(k) Number
FDA product code
HQF
EMDN code
Z12011011, Z12011017
GMDN term
General/multiple surgical frequency-doubled solid-state laser system
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
886.4390
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Size
Weight — 28 Kilogram

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Manufacturer details

EUDAMED SRN
TW-MF-000027493
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under LASER SURGERY INSTRUMENTS.

Other devices from Lightmed Corporation

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Properties

  • Reusable
  • Prescription use
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (18, all answered No)