# Retinapharma Technologies, Inc.

- Location (FDA's records): Rydal, PA
- FDA decisions: 1 (2004–2004): 1 510(k) clearance
- Product codes: HKX (1)
- Predicates its devices cite: 3 (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
- Oculab, Inc.: 1 (https://510kreport.com/company/oculab)
- Quantel Medical: 1 (https://510kreport.com/company/quantel-medical)
- Nidek, Inc.: 1 (https://510kreport.com/company/nidek)

## Recent decisions
- K042099: Tonopach Ultrasonic Tonometer/Pachymeter Model P-201 (the Tonopach) (Dec 10, 2004)

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