Konig Bell Circumcision Clamp
K-Number: K251687 · 2026-02-25
Device Summary
Frequently Asked Questions
What is the Konig Bell Circumcision Clamp?
Konig Bell Circumcision Clamp is a medical device that received FDA 510(k) clearance on 2026-02-25. The listed applicant is Medline Industries, LP. The 510(k) number is K251687.
When did Konig Bell Circumcision Clamp receive FDA 510(k) clearance?
Konig Bell Circumcision Clamp received FDA 510(k) clearance on 2026-02-25, under 510(k) number K251687.
Who is the listed applicant for Konig Bell Circumcision Clamp?
The FDA 510(k) record lists Medline Industries, LP as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Konig Bell Circumcision Clamp?
The FDA product code for Konig Bell Circumcision Clamp is HFX.
Other records listing Medline Industries, LP as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HFX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.