Hidrex GmbH
Hidrex GmbH holds FDA 510(k) medical device clearance, cleared in 2015, with 3 FDA device recalls on record.
Top product codes for Hidrex GmbH
FDA recalls by Hidrex GmbH
- Z-1238-2017 — Daavlin Aquex (DAAV1000)
- Z-1237-2017 — Hidrex USA DVP1000
- Z-1236-2017 — Hidrex USA DP450
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 Hidrex GmbH
Data sourced from openFDA. This site is unofficial and independent of the FDA.