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ARTAS System FP-25000

by Venus Concept Inc.

ARTAS System FP-25000 is a Class II device made by Venus Concept Inc., listed in FDA GUDID since 8 Jun 2023 (UDI-DI 00810060830079), 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

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810060830079 UDI-DI Date8 Jun 2023ListedStatusListed 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  • Withdrawn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
ARTAS System
Generic name
Robotic surgical telemanipulation system
Model / reference
FP-25000
Primary DI / UDI-DI
00810060830079
FDA product code
ONA
GMDN term
Robotic surgical telemanipulation system
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution

Related devices

Category: Robotic surgical arm system

Similar devices in this category

Other devices filed under Robotic surgical arm system.

Other devices from Venus Concept Inc.

See all devices from Venus Concept Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)