# Minilap Technologies

- Location (FDA's records): Dobbs Ferry, NY
- FDA decisions: 2 (2012–2013): 2 510(k) clearances
- Product codes: OCW (1), GEI (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 1 (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
- Mini Lap Technologies, Inc.: 2 (https://510kreport.com/company/mini-lap-technologies)
- Carefusion 2200, Inc.: 1 (https://510kreport.com/company/carefusion-2200)
- Aesculap, Inc.: 1 (https://510kreport.com/company/aesculap)
- Richard Wolf Medical Instruments Corp.: 1 (https://510kreport.com/company/richard-wolf-medical-instruments)

## Firms that cite its devices most
- Teleflexmedical, Inc.: 1 (https://510kreport.com/company/teleflexmedical)

## Its most-cited devices
- K113597: Mini-Lap Bipolar Electrocautery Devices (2012), cited by 1

## Recent decisions
- K132232: Mins Needlescopic Resposable Device System (Dec 4, 2013)
- K113597: Mini-Lap Bipolar Electrocautery Devices (Jun 3, 2012)

Source page: https://510kreport.com/company/minilap-technologies