# E Surgical, LLC

- Location (FDA's records): Boulder, CO
- FDA decisions: 5 (2006–2024): 5 510(k) clearances
- Product codes: GEI (4), HRX (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 2 (1 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
- Bovie Medical Corporation: 2 (https://510kreport.com/company/bovie-medical)
- Valleylab, Inc.: 1 (https://510kreport.com/company/valleylab)
- New Deantronics Taiwan, Ltd.: 1 (https://510kreport.com/company/new-deantronics-taiwan)
- Trice Medical, Inc.: 1 (https://510kreport.com/company/trice-medical)

## Firms that cite its devices most
- New Deantronics Taiwan, Ltd.: 1 (https://510kreport.com/company/new-deantronics-taiwan)

## Its most-cited devices
- K231126: Eblator Device (2023), cited by 1
- K060255: E Surgical Electrosurgical Patient Return Electrode, Dual Plate with Cord and Electrosurgical Patient Return Electrode (2006), cited by 1

## Recent decisions
- K233115: Hawkeye Control Unit with Eyas Endoscope (Feb 6, 2024)
- K231126: Eblator Device (Aug 2, 2023)
- K071080: Electrosurgical Infant Patient Return Electrode, Dual Plate with Cord, Model EP 211M (Aug 31, 2007)
- K061878: Electrode Coated Ball, Model AB302C; Needle, Model AN301C; Blade, Model AE301HC (Oct 24, 2006)
- K060255: E Surgical Electrosurgical Patient Return Electrode, Dual Plate with Cord and Electrosurgical Patient Return Electrode (Mar 31, 2006)

Source page: https://510kreport.com/company/e-surgical