MMK
- Product code
- MMK
- Device name
- Container, Sharps
- Device class
- Class 2
- 21 CFR
- 21 CFR 880.5570
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 6
- Summaries archived here
- 4 (direct download)
- 510(k) clearances (all years, FDA)
- 114 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (6)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K260845 | 2026-08-05 | Tianjin Huahong Technology Co., Ltd. | Huahong Sharps Container (HHR-I, HHR-II) | FDA |
| K253773 | 2026-05-22 | Taizhou Huangyan Guanhong Plastic Stee… | Guanhong Sharps Container (GHW-1F1); Guanhong Sharps… | |
| K253222 | 2025-12-22 | Zhejiang Gongdong Medical Technology C… | Gongdong Sharps Container (SCR-01Q, SCR-01G, SCR-03G… | FDA |
| K251874 | 2025-10-14 | Pureway Compliance, Inc. | PureWay Sharps Container 1-Gal, 2-Gal, 3-Gal (800011… | |
| K252637 | 2025-10-14 | Keter Canada, Inc. | Community Containers (Flap and Daisy) | |
| K231484 | 2023-09-14 | Pureway Compliance, Inc. | PureWay 1.4 Quart Sharps Collector |
Official FDA classification page: MMK
Classification and pathway per current FDA publications. Data from openFDA (CC0).