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 15, 2026, FDA's public records list Lares Manufacturing Co., Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 14, 1983: PERMALUX VISIBLE CURE COMPOSITE RESTOR.
| Nov 14, 1983 | PERMALUX VISIBLE CURE COMPOSITE RESTORK831351 · EBF | 510(k) clearances |
| Dec 16, 1980 | LARES HANDPIECE OILK801535 · EFB | 510(k) clearances |
| Jul 21, 1980 | FIBER OPTIC HOSEK801592 · EAY | 510(k) clearances |
| Jul 21, 1980 | FIBER OPTIC ILLUMINATORK801591 · EAY | 510(k) clearances |
| Jul 14, 1980 | LARES AIR PRESSURE GAUGEK801534 · EIA | 510(k) clearances |
| Jan 20, 1978 | DENTAL HANDPIECEK780038 · EFB | 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
