Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K160752Substantially Equivalent

HARMONIC HD 1000i Shears 20 cm Length, HARMONIC HD 1000i Shears 36 cm Length

Ethicon Endo-Suregery, LLC, Guaynabo PR / Traditional, Substantially Equivalent

K160752 is the FDA 510(k) clearance record for HARMONIC HD 1000i Shears 20 cm Length, HARMONIC HD 1000i Shears 36 cm Length, cleared for Ethicon Endo-Suregery, LLC on under FDA product code LFL (Instrument, Ultrasonic Surgical). FDA records list one 510(k) clearance for Ethicon Endo-Suregery, LLC. As of , FDA records show no recalls naming K160752.

Clearance record

Decision date
Received
(103 days to decision)
Product code
LFL Instrument, Ultrasonic Surgical
Device class
Unclassified
Review panel
Unknown
Applicant
Ethicon Endo-Suregery, LLC 475 Calle C, Guaynabo PR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LFL

Trailing 12 months
1 clearance under product code LFL in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LFL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260