Mirion Technologies (Capintec), Inc.
Mirion Technologies (Capintec), Inc. holds FDA 510(k) medical device clearance, cleared in 2026, with 4 FDA device recalls on record.
Top product codes for Mirion Technologies (Capintec), Inc.
FDA recalls by Mirion Technologies (Capintec), Inc.
- Z-1892-2024 — Captus 4000e Thyroid Uptake System. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests.
- Z-1893-2024 — Captus 4000e Thyroid Uptake System with Well. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests.
- Z-1894-2024 — Captus 4000e Thyroid Uptake System with Well and 2 inch shielding. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests.
- Z-1069-2024 — Captus 4000e Thyroid Uptake Systems- Intended to be used by trained Nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures. Models: 5430-30151, 5430-30152, and 5430-30154
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 Mirion Technologies (Capintec), Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.