Iba Dosimetry GmbH
Iba Dosimetry GmbH holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2020, with 5 FDA device recalls on record.
Top product codes for Iba Dosimetry GmbH
FDA recalls by Iba Dosimetry GmbH
- Z-1703-2025 — myQA iON; Article Number: MQ10-000;
- Z-0683-2016 — IBA Dosimetry GmbH Lift Table Type 4320, Catalog HA03-010#2 and HA03-000#2
- Z-1212-2015 — COMPASS SW Version 3.1, Catalog Number CS10-100, medical linear accelerator, radiological
- Z-0168-2015 — COMPASS, Model No. SW Version 3.1, catalogue number CS10-100 (medical Linear accelerator) radiological
- Z-0456-2014 — iba COMPASS SW Version 3.0, Catalog Number CS10-100 (medical linear accelerator) radiological
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 Iba Dosimetry GmbH
Data sourced from openFDA. This site is unofficial and independent of the FDA.