# Urologix, Inc.

- Location (FDA's records): Plymouth
- FDA decisions: 3 (1996–2015): 1 510(k) clearance and 2 original PMA approvals
- Names in FDA's records: Urologix, Inc. (2); Urologix, LLC (1)
- Product codes: MEQ (2), GEI (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)

## Firms that cite its devices most
- Nxthera, Inc.: 1 (https://510kreport.com/company/nxthera)

## Its most-cited devices
- K142248: Prostiva RF Therapy Generator, Prostiva RF Therapy Hand Piece, Prostiva RF Therapy Return Electrode, Prostiva RF Therapy Tubing System, Prostiva RF Therapy Telescope (2015), cited by 1

## Recent decisions
- K142248: Prostiva RF Therapy Generator, Prostiva RF Therapy Hand Piece, Prostiva RF Therapy Return Electrode, Prostiva RF Therapy Tubing System, Prostiva RF Therapy Telescope (Feb 20, 2015)
- P970008: Targis (T3) System (Aug 22, 1997)
- P950014: Prostatron (May 3, 1996)

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