# Techmedic Development International B.V.

- Location (FDA's records): Broek Op Langedijk, NL
- FDA decisions: 1 (2016–2016): 1 510(k) clearance
- Product codes: MHX (1)
- Predicates its devices cite: 5 (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
- Vitalconnect, Inc.: 1 (https://510kreport.com/company/vitalconnect)
- Scottcare Corporation: 1 (https://510kreport.com/company/scottcare)
- Nonin Medical, Inc.: 1 (https://510kreport.com/company/nonin-medical)
- Cincinnati Sub-Zero Products, Inc.: 1 (https://510kreport.com/company/cincinnati-sub-zero-products)
- Welch Allyn Protocol, Inc.: 1 (https://510kreport.com/company/welch-allyn-protocol)

## Recent decisions
- K152973: Dyna-Vision Telemonitoring System (Apr 29, 2016)

Source page: https://510kreport.com/company/techmedic-development-international
