Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list RetinaLabs.com with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 22, 2000: TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023….
| Dec 22, 2000 | TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025K003036 · KYG | 510(k) clearances |
| Oct 24, 2000 | PDT DOSECALCULATOR, MODEL 80000K000418 · NDC | 510(k) clearances |
| May 9, 2000 | VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIESK000457 · HMX | 510(k) clearances |
| May 8, 2000 | SILICONE OIL EXPRESS (INFUSION PAK), MODELS 10000, 10001, 10002, 10003K000420 · MRH | 510(k) clearances |
| May 8, 2000 | TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001K000416 · MPA | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
