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Velys 451611050

by Medos International Sàrl

Velys 451611050 is a Class II device made by Medos International Sàrl, listed in FDA GUDID since 28 Mar 2025 (UDI-DI 10705034643250), 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 Number10705034643250 UDI-DI Date28 Mar 2025ListedStatusListed 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  • Withdrawn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
Velys
Generic name
Optical surgical tracking system spatial marker, single-use
Model / Ref / Catalog
451611050
Primary DI / UDI-DI
10705034643250
FDA product code
OLO
GMDN term
Optical surgical tracking system spatial marker, single-use
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical optical-tracking spatial marker, single-use

Similar devices

Other devices filed under FDA product code OLO (Orthopedic stereotaxic instrument).

Other devices from Medos International SARL

See all devices from Medos International SARL →

Properties

  • Serial number
Other properties (14, all answered No)