# Triton Technology, Inc.

- Location (FDA's records): Salem, OH
- FDA decisions: 4 (1988–1993): 4 510(k) clearances
- Product codes: FCK (2), BYZ (1), DPT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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 that cite its devices most
- Olympus Optical Co., Ltd.: 1 (https://510kreport.com/company/olympus-optical)

## Its most-cited devices
- K911448: Multiple Biopsy Device-MBX (1991), cited by 1

## Recent decisions
- K932142: Suction Guillotine Device (Sep 24, 1993)
- K911448: Multiple Biopsy Device-MBX (Apr 16, 1991)
- K902883: Tissue/Polyp Trap System (Sep 12, 1990)
- K881303: Triton Model 100 Pulsed Doppler Blood Flowmeter (Nov 29, 1988)

Source page: https://510kreport.com/company/triton-technology