# Inntec, Inc.

- Location (FDA's records): Stoughton, WI
- FDA decisions: 3 (2005–2005): 3 510(k) clearances
- Product codes: MQF (2), MQE (1)
- Predicates its devices cite: 2 (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
- Fertility Technology Resources, Inc.: 1 (https://510kreport.com/company/fertility-technology-resources)
- Lifetek Medical, Inc.: 1 (https://510kreport.com/company/lifetek-medical)

## Recent decisions
- K052059: Iui Catheter, Model 9057 (Nov 22, 2005)
- K051742: Oocyte Retrieval Needle Set, Models 917-IH and 917-SH (Oct 7, 2005)
- K050521: Embryo Transfer Catheter with Accessory Stylet, Models 9018, 9023, 9018-S, 9023-S (May 2, 2005)

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