Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Dhason Brothers, Inc. — Predicate Candidate Screening

14 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

35 daysmedian FDA review time

35 days90th percentile

14clearances measured

K-number	Device	Applicant	Decided	Review days
K890156	IMPACTOR FOR FEMORAL HEAD	Dhason Brothers, Inc.	1989-02-13	35
K890165	FORCEPS-ORTHOPEDIC	Dhason Brothers, Inc.	1989-02-13	35
K890163	AUSTIN MOORE HALLOW CHISEL	Dhason Brothers, Inc.	1989-02-13	35
K890168	RETRACTOR, SELF-RETAINING	Dhason Brothers, Inc.	1989-02-13	35
K890158	RETRACTORS	Dhason Brothers, Inc.	1989-02-13	35
K890162	EXTRACTOR FOR AUSTIN MOORE FEMORAL HEAD	Dhason Brothers, Inc.	1989-02-13	35
K890161	THOMPSON TYPE RASP W/TOMMY BAR	Dhason Brothers, Inc.	1989-02-13	35
K890157	FORCEPS	Dhason Brothers, Inc.	1989-02-13	35
K890166	RONGUER-ORTHOPEDIC	Dhason Brothers, Inc.	1989-02-13	35
K890164	HUDSON BRACE W/BURRS	Dhason Brothers, Inc.	1989-02-13	35
K890160	GOUGES FOR FEMORAL HEADS	Dhason Brothers, Inc.	1989-02-13	35
K890167	HOLDER, NEEDLE	Dhason Brothers, Inc.	1989-02-03	25
K890170	SCISSORS	Dhason Brothers, Inc.	1989-02-03	25
K890159	TOWEL CLIPS	Dhason Brothers, Inc.	1989-02-03	25

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda