Propper Manufacturing Co., Inc.
Propper Manufacturing Co., Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 31, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K250306 | Chex-All Sterilization Pouches and Tubes | October 31, 2025 |
| K240910 | EO Chex Indicator Tape | June 12, 2024 |
| K222137 | OK Plus Indicator | December 5, 2022 |
| K212592 | Gas-Chex Indicator | January 20, 2022 |
| K210866 | Steri-Dot Process Indicator | June 21, 2021 |
| K210553 | Steam-Dot Process Indicator | May 19, 2021 |
| K141638 | PROPPER INSIGHT BINOCULAR INDIRECT OPHTHALMOSOPE | September 17, 2014 |