FDA applicant
Retinalabs.Com
FDA records 5 decisions for Retinalabs.Com (Atlanta, GA) in 2000: 5 510(k) clearances. Most are in product codes KYG (Device, Irrigation, Ocular Surgery) and HMX (Cannula, Ophthalmic). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Retinalabs.Com’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Retinalabs.Com since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Retinalabs.Com’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report