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 Aesthetic and Reconstructive Technologies with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jan 23, 2003: DIMISIL SCAR GEL.
| Jan 23, 2003 | DIMISIL SCAR GELK023678 · MDA | 510(k) clearances |
| Oct 10, 2002 | AART SILICONE TUBINGK022306 · KGZ | 510(k) clearances |
| Aug 26, 2002 | AART CALF IMPLANTK022511 · MIB | 510(k) clearances |
| Aug 8, 2002 | AART SILICONE SHEETINGK022223 · MIB | 510(k) clearances |
| Jul 16, 2002 | AART SILICONE CARVING BLOCKK021820 · MIB | 510(k) clearances |
| Jul 16, 2002 | AART GLUTEAL IMPLANTK021839 · MIB | 510(k) clearances |
| Jul 3, 2002 | AART PECTORALIS IMPLANTK021337 · MIC | 510(k) clearances |
| Jul 2, 2002 | AART MALAR IMPLANTK021419 · LZK | 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
