Laax, Inc.
Laax, Inc. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2011, with 2 FDA device recalls on record.
Top product codes for Laax, Inc.
FDA recalls by Laax, Inc.
- Z-1461-2015 — TIGERPAW System II, Part number C-TP-1507 (7 connector) The TigerPaw System II is an implantable occlusion Fastener to be placed on the Ostium of the Left Atrial Appendage (LAA).
- Z-1462-2015 — TIGERPAW System II, Part number C-TP-1509 (9 connector) The TigerPaw System II is an implantable occlusion Fastener to be placed on the Ostium of the Left Atrial Appendage (LAA).
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Laax, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.