510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K132124Substantially Equivalent

Klarity Vacuum Bag, Klarity Mold Cushion

Klarity Medical Products LLC, Newark OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K132124 is the FDA 510(k) clearance record for KLARITY VACUUM BAG, KLARITY MOLD CUSHION, a class II device, cleared for Klarity Medical Products, LLC on under FDA product code IYE (Accelerator, Linear, Medical). FDA records list one 510(k) clearance for Klarity Medical Products, LLC. As of , FDA records show one recall naming K132124.

Clearance record

Decision date
Received
(114 days to decision)
Product code
IYE Accelerator, Linear, Medical
Regulation
21 CFR 892.5050
Device class
Class II
Review panel
Radiology
Applicant
Klarity Medical Products, LLC 80 Westgate Dr., Newark OH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IYE

Trailing 12 months
16 clearances under product code IYE in the twelve months to October 2026, January 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code IYE, trailing twelve months
MonthClearances
November 20251
December 20251
January 20264
February 20260
March 20261
April 20262
May 20261
June 20262
July 20260
August 20263
September 20261
October 20260