510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K220411Substantially Equivalent

Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)

Stryker Sustainability Solutions, Tempe AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K220411 is the FDA 510(k) clearance record for Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A), a class II device, cleared for Stryker Sustainability Solutions on under FDA product code NUJ (Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed). FDA's definition for product code NUJ reads: "Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf)". FDA records list 88 510(k) clearances for Stryker Sustainability Solutions, from to . As of , FDA records show no recalls naming K220411.

Clearance record

Decision date
Received
(88 days to decision)
Product code
NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Regulation
21 CFR 878.4400
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Stryker Sustainability Solutions 1810 W Dr.Ake Dr., Tempe AZ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NUJ

Trailing 12 months

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

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