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 13, 2026, FDA's public records list LCA, Inc. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Aug 28, 1995: PADLESS ELECTROSURGICAL PENCIL.
| Date | Record | Source |
|---|---|---|
| Aug 28, 1995 | PADLESS ELECTROSURGICAL PENCILK952792 · GEI | 510(k) clearances |
| Oct 7, 1994 | THE HOOK-CURVED CLOSED END/ELECT FIBER LASER DELIV SYSK944091 · GEX | 510(k) clearances |
| Mar 7, 1994 | SNJ SMOKE EVACUATION SUCTION WANDK935439 · FYD | 510(k) clearances |
| Jan 13, 1994 | HYBRID SURGICAL DEVICE MODIFICATIONK935258 · GEX | 510(k) clearances |
| Nov 22, 1993 | ALLOY SCALPEL HANDPIECES, MODIFICATIONK925726 · GEX | 510(k) clearances |
| Oct 5, 1993 | CLOSED END FIBEROPTIC LASER DELIVERY SYSTEMK931070 · GEX | 510(k) clearances |
| Apr 23, 1993 | HYBRID SURGICAL DEVICEK924160 · GEX | 510(k) clearances |
| Mar 31, 1993 | ZOE LASER, CONTACT ND:YAG LASER SYSTEMK923991 · GEX | 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
