# Infrascan, Inc.

- Location (FDA's records): Philadelphia, PA
- FDA decisions: 5 (2011–2024): 4 510(k) clearances and 1 De Novo grant
- Product codes: OPT (5)
- Predicates its devices cite: 5 (5 its own); citations of its devices by later devices: 5 (5 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K120949: Infrascanner (2013), cited by 2
- K211617: Infrascanner (2022), cited by 1
- K200203: Infrascanner (2020), cited by 1
- DEN100002: Infrascanner, Model 1000 (2011), cited by 1

## Recent decisions
- K241389: Infrascanner Model 2500 (Model 2500) (Dec 12, 2024)
- K211617: Infrascanner (Feb 9, 2022)
- K200203: Infrascanner (Jul 10, 2020)
- K120949: Infrascanner (Jan 11, 2013)
- DEN100002: Infrascanner, Model 1000 (Dec 13, 2011)

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