Medartis, Inc.
Medartis, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2023, with 2 FDA device recalls on record.
Top product codes for Medartis, Inc.
FDA recalls by Medartis, Inc.
- Z-1821-2024 — APTUS 2.8 TriLock Screw 22mm, HD7, 1/Pkg. Metal bone fixation fastener used with the APTUS fixation system.
- Z-0150-2015 — APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Plates are indicated for fractures and osteotomies, in particular for the ulna.
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 Medartis, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.