Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Shaser with 10 510(k) clearances. The most recent is a 510(k) clearance dated May 27, 2015: Shaser Skin Beauty Intense Pulsed Light System Family for Acne.
| Date | Record | Source |
|---|---|---|
| May 27, 2015 | Shaser Skin Beauty Intense Pulsed Light System Family for AcneK150282 · ONF | 510(k) clearances |
| Feb 13, 2015 | Shaser Skin Beauty SkinREJUV Intense, Pulsed Light System FamilyK142924 · GEX | 510(k) clearances |
| Jul 22, 2014 | SHASER SKIN BEAUTY INTENSE PULSED LIGHT SYSTEM FAMILYK141583 · ONF | 510(k) clearances |
| May 16, 2014 | LUMENA FH HAIR REMOVAL SYSTEMK140631 · ONF | 510(k) clearances |
| Feb 12, 2014 | SHASER V-MINI 2 HAIR REMOVAL SYSTEMK133201 · ONF | 510(k) clearances |
| Nov 26, 2013 | SHASER V-MINI RXK132170 · ONF | 510(k) clearances |
| Sep 30, 2013 | SHASER HRS2 RX HAIR REMOVAL SYSTEMK132266 · ONF | 510(k) clearances |
| Jun 13, 2013 | SHASER V-MINI HAIR REMOVAL SYSTEMK130015 · ONF | 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
