510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K821278Substantially Equivalent

Hartman Forceps Straight 3 1/2

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

K821278 is the FDA 510(k) clearance record for HARTMAN FORCEPS STRAIGHT 3 1/2, a class I device, cleared for Conphar, Inc. on under FDA product code GEN (Forceps, General & Plastic Surgery). FDA records list 122 510(k) clearances for Conphar, Inc., from to . As of , FDA records show no recalls naming K821278.

Clearance record

Decision date
Received
(24 days to decision)
Product code
GEN Forceps, General & Plastic Surgery
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Conphar, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GEN

Trailing 12 months

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

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