# Incisive Technologies, Inc.

- Location (FDA's records): San Carlos, CA
- FDA decisions: 4 (1994–2023): 4 510(k) clearances
- Names in FDA's records: Incisive Technologies, Inc. (3); Incisive Technologies Pty, Ltd. (1)
- Product codes: GEX (3), LFC (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 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
- GreenMark Biomedical, Inc.: 1 (https://510kreport.com/company/greenmark-biomedical)

## Recent decisions
- K222560: BlueCheck™ Caries Detection & Monitoring (May 16, 2023)
- K945143: Dental Laser Fiber System (Nov 1, 1994)
- K943693: Pulsemaster S Series (Aug 22, 1994)
- K942217: Pulsejet Dental Laser System (Aug 3, 1994)

Source page: https://510kreport.com/company/incisive-technologies