# Profound Medical, Inc.

- Location (FDA's records): Mississauga, CA
- FDA decisions: 5 (2019–2024): 5 510(k) clearances
- Product codes: PLP (5)
- Predicates its devices cite: 4 (3 its own); citations of its devices by later devices: 3 (3 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
- Edap Technomed, Inc.: 1 (https://510kreport.com/company/edap-technomed)

## Its most-cited devices
- K191200: TULSA-PRO System (2019), cited by 3

## Recent decisions
- K240296: Tulsa Pro System (Pad-105) (May 9, 2024)
- K230692: TULSA-PRO System (Sep 20, 2023)
- K211858: TULSA-PRO System (Sep 6, 2022)
- K202286: Tulsa-Pro System (Sep 16, 2020)
- K191200: TULSA-PRO System (Aug 15, 2019)

Source page: https://510kreport.com/company/profound-medical