# Arvik Enterprises/ Mini Lap Technologies

- Location (FDA's records): Shelton, CT
- FDA decisions: 1 (2011–2011): 1 510(k) clearance
- Product codes: GAA (1)
- Predicates its devices cite: 1 (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
- Ximed/Prosure/Injectx: 1 (https://510kreport.com/company/ximed-prosure-injectx)

## Recent decisions
- K102274: Arvik Laparoscopic Aspiration Instrument (Jun 15, 2011)

Source page: https://510kreport.com/company/arvik-enterprises-mini-lap-technologies