# Mectra Labs, Inc.

- Location (FDA's records): Bloomfield, IN
- FDA decisions: 9 (1992–2012): 9 510(k) clearances
- Product codes: HIF (3), GEI (2), GCJ (2), HIN (1), OCT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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 that cite its devices most
- Smiths Medical: 1 (https://510kreport.com/company/smiths-medical)
- STERIS Corporation: 1 (https://510kreport.com/company/steris)
- New Wave Surgical Corporation: 1 (https://510kreport.com/company/new-wave-surgical)
- Patton Surgical Corp.: 1 (https://510kreport.com/company/patton-surgical)

## Its most-cited devices
- K033880: Electro-Lube (2004), cited by 2
- K021247: Pneumoperitoneum Insufflation Needle (2002), cited by 1
- K993604: Endoscopic Anti Fog Device (2000), cited by 1

## Recent decisions
- K113080: Tubalgator (Jun 29, 2012)
- K033880: Electro-Lube (Mar 10, 2004)
- K021247: Pneumoperitoneum Insufflation Needle (Nov 8, 2002)
- K993604: Endoscopic Anti Fog Device (Mar 3, 2000)
- K955352: Suction Cautery Probe (Apr 5, 1996)
- K934547: Mectra Trocar (Feb 18, 1994)
- K935382: Graspers (Feb 15, 1994)
- K925691: Insufflation Tubing (Sep 23, 1993)

Source page: https://510kreport.com/company/mectra-labs