Arcoma AB
Arcoma AB holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2014, with 2 FDA device recalls on record.
Top product codes for Arcoma AB
FDA recalls by Arcoma AB
- Z-1332-2022 — Omnera 400A Digital Radiographic System
- Z-1331-2022 — Omnera 400T Digital Radiographic System
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 Arcoma AB
Data sourced from openFDA. This site is unofficial and independent of the FDA.