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 15, 2026, FDA's public records list Biophotas, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 2023: Biophotas Celluma CONTOUR.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Nov 21, 2023 | Biophotas Celluma CONTOURK232977 · OLI | 510(k) clearances |
| Jun 29, 2021 | Biophotas Celluma RESTOREK211038 · OAP | 510(k) clearances |
| Sep 1, 2017 | BIOPHOTAS CELLUMA3K171323 · OHS | 510(k) clearances |
| Mar 2, 2016 | BioPhotas Celluma3K152280 · ILY | 510(k) clearances |
| Jan 15, 2014 | BIOPHOTAS CELLUMAK131113 · ILY | 510(k) clearances |
| Jan 3, 2013 | BIOPHOTAS LIFELIGHTK122237 · ILY | 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
