510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K042341Substantially Equivalent

Ultraclip II US

Inrad, Kentwood MI / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K042341 is the FDA 510(k) clearance record for ULTRACLIP II US, a class II device, cleared for Inrad on under FDA product code NEU (Marker, Radiographic, Implantable). FDA records list 14 510(k) clearances for Inrad, from to . As of , FDA records show no recalls naming K042341.

Clearance record

Decision date
Received
(21 days to decision)
Product code
NEU Marker, Radiographic, Implantable
Regulation
21 CFR 878.4300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Inrad 4375 Donker Ct. SE, Kentwood MI
510(k) summary
Statement
Third party review
No

Clearances, product code NEU

Trailing 12 months
4 clearances under product code NEU in the twelve months to October 2026, December 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code NEU, trailing twelve months
MonthClearances
November 20250
December 20253
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260