HFX
- Product code
- HFX
- Device name
- Clamp, Circumcision
- Device class
- Class 2
- 21 CFR
- 21 CFR 884.4530
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 27
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name |
|---|---|---|---|
| K251687 | 2026-02-25 | Medline Industries, LP | Konig Bell Circumcision Clamp summary |
Official FDA classification page: HFX
Classification and pathway per current FDA publications. Data from openFDA (CC0).