510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K151095Substantially Equivalent

Circumplast Circumcision Device

Novadien Healthcare, Mount Lewis, AU / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K151095 is the FDA 510(k) clearance record for Circumplast Circumcision Device, a class II device, cleared for Novadien Healthcare on under FDA product code HFX (Clamp, Circumcision). FDA records list one 510(k) clearance for Novadien Healthcare. As of , FDA records show no recalls naming K151095.

Clearance record

Decision date
Received
(148 days to decision)
Product code
HFX Clamp, Circumcision
Regulation
21 CFR 884.4530
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Novadien Healthcare P.O. Box 7070, Mount Lewis, AU
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HFX

Trailing 12 months
1 clearance under product code HFX in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HFX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260