510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K965026Substantially Equivalent

Pfingst Pressure Paste

Pfingst & Co., Inc., South Plainfield, NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K965026 is the FDA 510(k) clearance record for PFINGST PRESSURE PASTE, a class I device, cleared for Pfingst & Co., Inc. on under FDA product code EFH (Paper, Articulation). FDA records list one 510(k) clearance for Pfingst & Co., Inc. As of , FDA records show no recalls naming K965026.

Clearance record

Decision date
Received
(55 days to decision)
Product code
EFH Paper, Articulation
Regulation
21 CFR 872.6140
Device class
Class I
Review panel
Dental
Applicant
Pfingst & Co., Inc. 105 Snyder Rd., South Plainfield, NJ
510(k) summary
Statement
Third party review
No

Clearances, product code EFH

Trailing 12 months

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

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