FDA applicant
Weinmann Emergency Medical Technology GmbH + Co. KG
FDA records 1 decision for Weinmann Emergency Medical Technology GmbH + Co. KG (Hamburg, DE) in 2020: 1 510(k) clearance. All are in product code BTL (Ventilator, Emergency, Powered (Resuscitator)). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Weinmann Emergency Medical Technology GmbH + Co. KG’s devices, and how often a recall has named them.
FDA decisions per year
1in 2020
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2020.
Planning a device like Weinmann Emergency Medical Technology…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Weinmann”
FDA records each applicant name separately; these may or may not be the same firm.