# Iogyn, Inc.

- Location (FDA's records): Cupertino, CA
- FDA decisions: 3 (2013–2014): 2 510(k) clearances and 1 De Novo grant
- Product codes: PGT (2), HIH (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 2 (1 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
- Henke Sass Wolf of America, Inc.: 1 (https://510kreport.com/company/henke-sass-wolf-of-america)
- Blazejewski Medi-Tech GmbH: 1 (https://510kreport.com/company/blazejewski-medi-tech)

## Firms that cite its devices most
- Minerva Surgical, Inc.: 1 (https://510kreport.com/company/minerva-surgical)

## Its most-cited devices
- DEN130040: Iogyn System (2014), cited by 1
- K141848: Iogyn System (2014), cited by 1

## Recent decisions
- K141848: Iogyn System (Aug 29, 2014)
- DEN130040: Iogyn System (Mar 28, 2014)
- K123330: Iogyn Endoscope (Mar 19, 2013)

Source page: https://510kreport.com/company/iogyn