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 Prowess Inc. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Dec 15, 2023: Panther TPS.
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.
| Date | Record | Source |
|---|---|---|
| Dec 15, 2023 | Panther TPSK231825 · MUJ | 510(k) clearances |
| Sep 28, 2021 | Panther OISK211760 · IYE | 510(k) clearances |
| Apr 27, 2020 | Panther StereotacticK193459 · MUJ | 510(k) clearances |
| Dec 11, 2015 | Panther StereoSeedK143514 · MUJ | 510(k) clearances |
| Dec 21, 2012 | PANTHER OIS/R & V MODEL VERSION 2.0K122616 · IYE | 510(k) clearances |
| Jul 27, 2010 | PROWESS PANTHER PROARC, MODEL VERSION 5.0K101076 · MUJ | 510(k) clearances |
| Jun 18, 2010 | PUMA MODEL VERSION 1.0K100801 · IYE | 510(k) clearances |
| May 5, 2009 | PANTHER REALART, MODEL 4.7K083502 · MUJ | 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
