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 Aesthetech Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 25, 1987: CREAT BRAND O-RISE GENERAL ASPIRATOR.
| Date | Record | Source |
|---|---|---|
| Nov 25, 1987 | CREAT BRAND O-RISE GENERAL ASPIRATORK873940 · BTA | 510(k) clearances |
| Sep 11, 1987 | CREAT BRAND MALAR IMPLANTK873434 · LZK | 510(k) clearances |
| Sep 24, 1985 | CREAT BRAND I/A PACK CREAT BRAND PHACO PACKK853189 · HQC | 510(k) clearances |
| Nov 6, 1984 | CREAT BRAND SKIN EXPANDERK843678 · LCJ | 510(k) clearances |
| Apr 24, 1984 | DISPOSABLE SUCTION TUBING SETK841283 · | 510(k) clearances |
| Sep 11, 1981 | CREAT BRAND WAGNER CHIN IMPLANTK812210 · FWP | 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
