510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K771106Substantially Equivalent

Forceps, Ob, Non-Compressive

Zeppelin Medizinlechnik GmbH, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K771106 is the FDA 510(k) clearance record for FORCEPS, OB, NON-COMPRESSIVE, a class II device, cleared for Zeppelin Medizinlechnik GmbH on under FDA product code HDA (Forceps, Obstetrical). FDA records list one 510(k) clearance for Zeppelin Medizinlechnik GmbH. As of , FDA records show no recalls naming K771106.

Clearance record

Decision date
Received
(11 days to decision)
Product code
HDA Forceps, Obstetrical
Regulation
21 CFR 884.4400
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Zeppelin Medizinlechnik GmbH 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HDA

Trailing 12 months

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

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