# Arstasis, Inc.

- Location (FDA's records): Redwood City, CA
- FDA decisions: 14 (2010–2015): 14 510(k) clearances
- Product codes: DYB (12), DRE (2)
- Predicates its devices cite: 22 (14 its own); citations of its devices by later devices: 14 (14 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Merit Medical Systems, Inc.: 3 (https://510kreport.com/company/merit-medical-systems)
- Cardiva Medical, Inc.: 2 (https://510kreport.com/company/cardiva-medical)
- Terumo Medical Corp.: 1 (https://510kreport.com/company/terumo-medical)
- Cordis Corp.: 1 (https://510kreport.com/company/cordis)
- Togo Medikit Co., Ltd.: 1 (https://510kreport.com/company/togo-medikit)

## Its most-cited devices
- K132263: Axera 2 Access System (2013), cited by 2
- K123135: Axera 2 Access System Model AXE200 (2013), cited by 2
- K140201: Axera 2 Access System (2014), cited by 1
- K100615: Arstasis Access System (2010), cited by 1
- K123618: Axera 2 Access System (2013), cited by 1
- K140287: Axera RX Access System (2014), cited by 1

## Recent decisions
- K151877: MicroTract Access System (Aug 7, 2015)
- K140871: Axera 2 Access System (Jun 6, 2014)
- K140287: Axera RX Access System (May 16, 2014)
- K140201: Axera 2 Access System (Mar 28, 2014)
- K132263: Axera 2 Access System (Aug 19, 2013)
- K123618: Axera 2 Access System (Mar 24, 2013)
- K123135: Axera 2 Access System Model AXE200 (Jan 28, 2013)
- K121521: Axera Access System (Jun 21, 2012)

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