510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K890156Substantially Equivalent

Impactor for Femoral Head

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

K890156 is the FDA 510(k) clearance record for IMPACTOR FOR FEMORAL HEAD, a class I device, cleared for Dhason Brothers, Inc. on under FDA product code LXH (Orthopedic Manual Surgical Instrument). FDA records list 14 510(k) clearances for Dhason Brothers, Inc., from to . As of , FDA records show no recalls naming K890156.

Clearance record

Decision date
Received
(35 days to decision)
Product code
LXH Orthopedic Manual Surgical Instrument
Regulation
21 CFR 888.4540
Device class
Class I
Review panel
Orthopedic
Applicant
Dhason Brothers, Inc. 1705 Merrimak Dr., Hyattsville MD
Third party review
No

Clearances, product code LXH

Trailing 12 months

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

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