# Electroscope, Inc.

- Location (FDA's records): Boulder, CO
- FDA decisions: 6 (1991–2000): 6 510(k) clearances
- Product codes: GEI (6)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 12 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Encision, Inc.: 3 (https://510kreport.com/company/encision)

## Its most-cited devices
- K912780: Monopolar Laparoscopic Electrodes W/Eletroshield (1991), cited by 2
- K913625: Electroscope Monitor, EM-1 (1991), cited by 1

## Recent decisions
- K000480: Active Electrode Monitoring System (May 2, 2000)
- K972562: Bipolar Electrosurgical Pencil, Straight and Angled (Jan 16, 1998)
- K973682: Bipolar Arthroscopic Probe, Straight, Biopolar Arthroscopic Probe, Angled, Bipolar Arthroscopic Probe, Straight, (Dec 18, 1997)
- K912780: Monopolar Laparoscopic Electrodes W/Eletroshield (Dec 30, 1991)
- K912781: Electroshield (Dec 30, 1991)
- K913625: Electroscope Monitor, EM-1 (Dec 30, 1991)

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