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

J. Jamner Surgical Instruments, Inc. · Predicate Candidate Screening

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

127 daysmedian FDA review time

208 days90th percentile

11clearances measured

K-number	Device	Applicant	Decided	Review days	Recalls (K-match)
K082349	JARIT HULKA UTERINE TENACULUM FORCEPS	J. Jamner Surgical Instruments, Inc.	2008-11-21	98	1
K944670	JARIT RECOMMENDED SINUS INSTRUMENTS	J. Jamner Surgical Instruments, Inc.	1995-02-02	133	0
K944870	JARIT ENDOSCOPES, MODELS 600-600; 600-630; 600-650; AND 600-	J. Jamner Surgical Instruments, Inc.	1994-11-02	41	0
K941565	JARIT RECOMMENDED SINUS INSTRUMENTS	J. Jamner Surgical Instruments, Inc.	1994-05-16	45	0
K932456	JARIT SURGICAL INSTRUMENTS	J. Jamner Surgical Instruments, Inc.	1994-04-21	335	1
K933728	JARIT SURGICAL INSTRUMENTS: CATALOG 615-330, 615-331, 615-33	J. Jamner Surgical Instruments, Inc.	1994-02-23	205	0
K931928	JARIT SURGICAL INSTRUMENTS	J. Jamner Surgical Instruments, Inc.	1993-11-10	208	0
K931959	JARIT SURGICAL INSTRUMENTS	J. Jamner Surgical Instruments, Inc.	1993-10-05	167	0
K931878	JARIT ENDOSCOPES, 600-600; 600-630; 600-650; 680	J. Jamner Surgical Instruments, Inc.	1993-08-19	127	0
K771625	LEININGEO AORTIC PUNCH #310-395 & 397	J. Jamner Surgical Instruments, Inc.	1977-09-12	18	0
K771624	COPE LUNG FORCEPS #305-218	J. Jamner Surgical Instruments, Inc.	1977-09-06	12	0

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