510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K952889Substantially Equivalent

Insul-Coat/2 Ceramic Coated Endo Medical Instruments

Materials Conversion Corp., Wheeling IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K952889 is the FDA 510(k) clearance record for INSUL-COAT/2 CERAMIC COATED ENDO MEDICAL INSTRUMENTS, a class II device, cleared for Materials Conversion Corp. on under FDA product code HET (Laparoscope, Gynecologic (And Accessories)). FDA records list one 510(k) clearance for Materials Conversion Corp. As of , FDA records show no recalls naming K952889.

Clearance record

Decision date
Received
(182 days to decision)
Product code
HET Laparoscope, Gynecologic (And Accessories)
Regulation
21 CFR 884.1720
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Materials Conversion Corp. 236-B Egidi Dr., Wheeling IL
510(k) summary
Summary
Third party review
No

Clearances, product code HET

Trailing 12 months

FDA records hold no clearances under product code HET in the trailing twelve months.

FDA records show no clearances under product code HET in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HET, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260