FDA Device Intelligence
HomeVenus Concept Inc. › ARTAS iX

ARTAS iX

Venus Concept Inc. · Model System · UDI-DI 00810060831632

ONA
1
510(k) clearances
2
Adverse events
4
Recalls
2
Facilities

Recalls

DateFirmReason
2013-10-13Restoration RoboticsReports of discoloration (residue) on the pins of the skin tensioner have been received by several customers. Discoloration due to insufficient cleaning of stainless steel pins dur
2013-10-13Restoration RoboticsReports of discoloration (residue) on the pins of the skin tensioner have been received by several customers. Discoloration due to insufficient cleaning of stainless steel pins dur
2013-10-13Restoration RoboticsReports of discoloration (residue) on the pins of the skin tensioner have been received by several customers. Discoloration due to insufficient cleaning of stainless steel pins dur
2013-10-13Restoration RoboticsReports of discoloration (residue) on the pins of the skin tensioner have been received by several customers. Discoloration due to insufficient cleaning of stainless steel pins du

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.