510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K833241Substantially Equivalent

Intrex

Pennwalt Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K833241 is the FDA 510(k) clearance record for INTREX, a class II device, cleared for Pennwalt Corp. on under FDA product code EAP (Unit, X-Ray, Intraoral). FDA records list 6 510(k) clearances for Pennwalt Corp., from to . As of , FDA records show no recalls naming K833241.

Clearance record

Decision date
Received
(67 days to decision)
Product code
EAP Unit, X-Ray, Intraoral
Regulation
21 CFR 872.1810
Device class
Class II
Review panel
Dental
Applicant
Pennwalt Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EAP

Trailing 12 months

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

FDA records show no clearances under product code EAP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EAP, 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