# Avenir Performance Europeenne Medical (Apem)

- Location (FDA's records): Château-Landon, FR
- FDA decisions: 3 (2019–2022): 3 510(k) clearances
- Names in FDA's records: Avenir Performance Europeenne Medical (Apem) (2); Avenir Performance Européenne Medical (Apem) (1)
- Product codes: LHI (3)
- 510(k) review time since 2016: median 235 days, against 247 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medimop Medical Project, Ltd.: 2 (https://510kreport.com/company/medimop-medical-project)

## Recent decisions
- K220856: Vial Adapter Ø13mm (Jun 21, 2022)
- K190816: Vial Adapter Ø20 mm , Vial Adapter Ø13 mm (Nov 19, 2019)
- K190149: Vial Adapter Ø20 mm (Oct 15, 2019)

Source page: https://510kreport.com/company/avenir-performance-europeenne-medical-apem