# Invatec S.P.A.

- Location (FDA's records): Bethlehem, PA
- FDA decisions: 4 (2009–2010): 4 510(k) clearances
- Product codes: LIT (2), FGE (1), NTE (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Invatec Innovative Technologies, S.R.L.: 2 (https://510kreport.com/company/invatec-innovative-technologies)
- Cordis Corp.: 2 (https://510kreport.com/company/cordis)
- Cordis Europa, N.V.: 1 (https://510kreport.com/company/cordis-europa)
- Medtronic Ave, Inc.: 1 (https://510kreport.com/company/medtronic-ave)
- W. L. Gore & Associates, Inc.: 1 (https://510kreport.com/company/w-l-gore-associates)

## Firms that cite its devices most
- Medtronic Vascular: 2 (https://510kreport.com/company/medtronic-vascular)
- Medtronic, Inc.: 2 (https://510kreport.com/company/medtronic)
- Abbott Vascular: 1 (https://510kreport.com/company/abbott-vascular)

## Its most-cited devices
- K100921: Admiral Xtreme Pta Balloon Dilatation Catheter (2010), cited by 3
- K092361: Reef HP 0.035 Otw Pta Balloon Dilatation Catheter (2009), cited by 2

## Recent decisions
- K100921: Admiral Xtreme Pta Balloon Dilatation Catheter (Apr 30, 2010)
- K092352: Scuba Biliary Stent System (Mar 16, 2010)
- K092361: Reef HP 0.035 Otw Pta Balloon Dilatation Catheter (Oct 29, 2009)
- K092177: MO.MA Ultra Proximal Cerebral Protection Device, Model MUS0130069X6 (Oct 15, 2009)

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