# Vidamed, Inc.

- Location (FDA's records): Menlo Park, CA
- FDA decisions: 11 (1995–2002): 11 510(k) clearances
- Product codes: GEI (7), KNS (4)
- Predicates its devices cite: 7 (7 its own); citations of its devices by later devices: 21 (7 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medtronic Vascular: 7 (https://510kreport.com/company/medtronic-vascular)
- Surx, Inc.: 3 (https://510kreport.com/company/surx)
- Argomed, Inc.: 3 (https://510kreport.com/company/argomed)
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)

## Its most-cited devices
- K960918: Vidamed Tuna (Transurethral Needle Ablation) System (1996), cited by 5
- K002583: Tuna (Trans Urethra Needle) Office System (2001), cited by 4
- K951245: Vidamed 50 Electrosurgical Generator, Vidamed Aec (Adjustable Electrosurgical Cartridge) Accessory (1995), cited by 3
- K014224: Precision Plus Tuna Office System (2002), cited by 2
- K965061: Vidamed Modedl 7600 RF Generator (1997), cited by 2
- K955035: Vidamed Series 7205 Electrosurgical Generator (1995), cited by 2

## Recent decisions
- K014224: Precision Plus Tuna Office System (Jan 23, 2002)
- K012587: RF Generators, Disposable Cartridge Kit, Disposable Cartridge, Reusable Handle, Disoisable Handpiece Reusable Telescope (Dec 11, 2001)
- K011787: Precision Tuna Office System with NO Rectal Temperature Monitoring Tape (Jul 6, 2001)
- K002583: Tuna (Trans Urethra Needle) Office System (Feb 13, 2001)
- K973366: Cobra Hand Piece (Nov 26, 1997)
- K965199: Tuna 5 Catheter (Apr 30, 1997)
- K965061: Vidamed Modedl 7600 RF Generator (Jan 28, 1997)
- K963180: Vidamed RF Generator Data Recorder (Oct 10, 1996)

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