# Trylon Corp.

- Location (FDA's records): Torrance, CA
- FDA decisions: 7 (1995–2004): 7 510(k) clearances
- Product codes: MPU (2), EAZ (2), HIC (1), HET (1), HFB (1)
- Predicates its devices cite: 2 (2 its own); citations of its devices by later devices: 6 (2 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Addent, Inc.: 2 (https://510kreport.com/company/addent)
- Remicalm, LLC: 1 (https://510kreport.com/company/remicalm)
- Led Medical Diagnostics, Inc.: 1 (https://510kreport.com/company/led-medical-diagnostics)

## Its most-cited devices
- K003995: Speculite/Orallite (2001), cited by 3
- K012070: Orallite Comprehensive Exam Tray (2001), cited by 2
- K033033: Vizilite-Blue Oral Exam Kit (2004), cited by 1

## Recent decisions
- K033033: Vizilite-Blue Oral Exam Kit (Nov 22, 2004)
- K011488: Spirabrush CX Biopsy Instrument (Feb 22, 2002)
- K012070: Orallite Comprehensive Exam Tray (Nov 27, 2001)
- K003995: Speculite/Orallite (Mar 16, 2001)
- K963391: Speculite (Dec 12, 1997)
- K955790: Pap Plus Speculoscopy Comprehensive Pelvic Exam Tray (Mar 21, 1996)
- K953364: Speculite (Dec 8, 1995)

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