510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K890165Substantially Equivalent

Forceps-Orthopedic

Dhason Brothers, Inc., Hyattsville MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890165 is the FDA 510(k) clearance record for FORCEPS-ORTHOPEDIC, a class I device, cleared for Dhason Brothers, Inc. on under FDA product code LXN (Probe, Test, Heart-Valve). FDA records list 14 510(k) clearances for Dhason Brothers, Inc., from to . As of , FDA records show no recalls naming K890165.

Clearance record

Decision date
Received
(35 days to decision)
Product code
LXN Probe, Test, Heart-Valve
Regulation
21 CFR 870.4500
Device class
Class I
Review panel
Cardiovascular
Applicant
Dhason Brothers, Inc. 1705 Merrimak Dr., Hyattsville MD
Third party review
No

Clearances, product code LXN

Trailing 12 months

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

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