# K251687: Konig Bell Circumcision Clamp

- Pathway: 510(k) (Traditional)
- Applicant: Medline Industries, LP
- Decided: Feb 25, 2026 after 268 days
- Product code: HFX (Clamp, Circumcision)
- Device class: 2
- Regulation: 21 CFR 884.4530
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K890897 (1989). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040052: Fine Surgical Circumcision Clamp, Fine Surgical Instrument Corp. (2004) Summary page 5.

## Indications for use
The Konig Bell Circumcision clamps are reusable instruments used in a procedure to compress the foreskin of the penis during the circumcision of male infant or child. Use of the Konig Bell Circumcision clamps in adults is to assist in Human Immunodeficiency Virus (HIV) prevention.

Source page: https://510kreport.com/device/K251687
Methodology: https://510kreport.com/methodology