# Retinalabs.Com

- Location (FDA's records): Atlanta, GA
- FDA decisions: 5 (2000–2000): 5 510(k) clearances
- Product codes: KYG (1), HMX (1), MRH (1), NDC (1), MPA (1)
- Predicates its devices cite: 0 (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

## Recent decisions
- K003036: Turbo-Flow Infusion Cannula 19 Gage,20 Gage,23 Gage, 25 Gage, Model 101019,101020,101023,101025 (Dec 22, 2000)
- K000418: PDT Dosecalculator, Model 80000 (Oct 24, 2000)
- K000457: Vertefusion-Photodynamic Therapy Pak, Model 11000 Series; Photofusion-Photodynamic Therapy Pak, Model 12000 Series (May 9, 2000)
- K000420: Silicone Oil Express (Infusion Pak), Models 10000, 10001, 10002, 10003 (May 8, 2000)
- K000416: Transpak (Vitreoretinal Infusion Pak), Models 90000, 90001 (May 8, 2000)

Source page: https://510kreport.com/company/retinalabs-com