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 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Propper Manufacturing with 32 510(k) clearances. The most recent is a 510(k) clearance dated Oct 31, 2025: Chex-All Sterilization Pouches and Tubes.
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 |
|---|---|---|
| Oct 31, 2025 | Chex-All Sterilization Pouches and TubesK250306 · FRG | 510(k) clearances |
| Jun 12, 2024 | EO Chex Indicator TapeK240910 · JOJ | 510(k) clearances |
| Dec 5, 2022 | OK Plus IndicatorK222137 · JOJ | 510(k) clearances |
| Jan 20, 2022 | Gas-Chex IndicatorK212592 · JOJ | 510(k) clearances |
| Jun 21, 2021 | Steri-Dot Process IndicatorK210866 · JOJ | 510(k) clearances |
| May 19, 2021 | Steam-Dot Process IndicatorK210553 · JOJ | 510(k) clearances |
| Sep 17, 2014 | PROPPER INSIGHT BINOCULAR INDIRECT OPHTHALMOSOPEK141638 · HLI | 510(k) clearances |
| Apr 5, 2012 | STEAM DOT BLU PROCESS INDICATORK111453 · JOJ | 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
