Konig Bell Circumcision Clamp
K-Number: K251687 · 2026-02-25
ApplicantMedline Industries, LP
Decision Date2026-02-25
Product CodeHFX
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
Konig Bell Circumcision Clamp is a medical device manufactured by Medline Industries, LP. It received FDA 510(k) clearance on 2026-02-25 under approval number K251687. The device is classified under product code HFX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Medline Industries, LP. The 510(k) number is K251687.
When was Konig Bell Circumcision Clamp approved by the FDA?
Konig Bell Circumcision Clamp received FDA 510(k) clearance on 2026-02-25, under approval number K251687.
What company makes Konig Bell Circumcision Clamp?
Konig Bell Circumcision Clamp is manufactured by Medline Industries, LP.
What is the FDA product code for Konig Bell Circumcision Clamp?
The FDA product code for Konig Bell Circumcision Clamp is HFX.
Other Devices by Medline Industries, LP
Related Devices (Code: HFX)
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.