510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K131282Substantially Equivalent

Nexus Hemorrhoid Ligator

Inx Medical, Chesterfield MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K131282 is the FDA 510(k) clearance record for NEXUS HEMORRHOID LIGATOR, a class II device, cleared for Inx Medical on under FDA product code FHN (Ligator, Hemorrhoidal). FDA records list one 510(k) clearance for Inx Medical. As of , FDA records show no recalls naming K131282.

Clearance record

Decision date
Received
(66 days to decision)
Product code
FHN Ligator, Hemorrhoidal
Regulation
21 CFR 876.4400
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Inx Medical 1819 Clarkson Rd., Chesterfield MO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FHN

Trailing 12 months

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

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