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

Martin Medical · Predicate Candidate Screening

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

17 daysmedian FDA review time

83 days90th percentile

14clearances measured

K-number	Device	Applicant	Decided	Review days
K873723	PLASTER VACUUM, 230V MODEL NO. 4183-161	Martin Medical	1987-12-10	86
K873721	PLASTER VACUUM, 115V MODEL NO. 4183-160	Martin Medical	1987-12-07	83
K873719	CAST CUTTER, 115V MODEL NO. 4183-106	Martin Medical	1987-10-02	17
K873716	ADULT WALKING HEEL PRODUCT NO. 4183-130	Martin Medical	1987-10-02	17
K873722	PEDESTAL WALKING HEEL PRODUCT NO. 4183-133	Martin Medical	1987-10-02	17
K873720	CAST CUTTER, 230V MODEL NO. 4183-107	Martin Medical	1987-10-02	17
K873718	CHILD WALKING HEEL PRODUCT NO. 4183-132	Martin Medical	1987-10-02	17
K873717	CUSHION TREAD WALKING HEEL PRODUCT NO. 4183-135	Martin Medical	1987-10-02	17
K863273	MARTIN MEDICAL PRO-SCOPE ANOSCOPE	Martin Medical	1986-11-04	71
K863274	MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM	Martin Medical	1986-09-02	8
K863275	MARTIN MEDICAL PRO-SPEC SMALL VAGINAL SPECULUM	Martin Medical	1986-09-02	8
K861075	AMERICAN ORTHOPAEDIC CAST CUTTER, MODEL 0295-202	Martin Medical	1986-03-28	7
K861073	AMERICAN ORTHOPAEDIC VACUUM 0295-250	Martin Medical	1986-03-28	7
K861074	AMERICAN ORTHOPAEDIC CAST CUTTER, MODEL 0295-200	Martin Medical	1986-03-28	7

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