Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

Kinetic Medical Products · Predicate Candidate Screening

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

9 daysmedian FDA review time

24 days90th percentile

63clearances measured

K-number	Device	Applicant	Decided	Review days
K890385	MIDWIFERY/OBSTETRICAL FORCEPS	Kinetic Medical Products	1989-03-01	37
K890376	VAGINAL SPECULUM	Kinetic Medical Products	1989-02-27	35
K890380	CERVICAL BIOPSY FORCEPS	Kinetic Medical Products	1989-02-27	35
K890382	COMPRESSION FORCEPS	Kinetic Medical Products	1989-02-27	35
K890387	MALLEABLE PLACENTA CURETTE	Kinetic Medical Products	1989-02-27	35
K890216	MICROSURGICAL KERATOME	Kinetic Medical Products	1989-02-16	29
K890383	HYSTERECTOMY FORCEPS	Kinetic Medical Products	1989-02-16	24
K890375	VAGINAL SPECULUM	Kinetic Medical Products	1989-02-13	21
K890377	FIXED-SIZE UTERINE DILATOR	Kinetic Medical Products	1989-02-13	21
K890378	UTERINE DRESSING FORCEPS	Kinetic Medical Products	1989-02-13	21
K890379	UTERINE TENTACULUM	Kinetic Medical Products	1989-02-13	21
K890384	UTERINE CURETTE	Kinetic Medical Products	1989-02-13	21
K890386	PLACENTA AND OVUM FORCEPS	Kinetic Medical Products	1989-02-13	21
K890388	CEPHALOTOMY SCISSORS	Kinetic Medical Products	1989-02-13	21
K890389	UMBILICAL SCISSORS	Kinetic Medical Products	1989-02-13	21
K890235	DRESSING SCISSORS	Kinetic Medical Products	1989-02-03	16
K890365	SEPTUM ELEVATOR	Kinetic Medical Products	1989-02-03	11
K890366	ADENOID CURETTE	Kinetic Medical Products	1989-02-03	11
K890368	KIDNEY CLAMP	Kinetic Medical Products	1989-02-03	11
K890369	GALL STONE FORCEPS	Kinetic Medical Products	1989-02-03	11
K890371	INTESTINAL CRUSHING CLAMP	Kinetic Medical Products	1989-02-03	11
K890372	INTESTINAL CLAMP	Kinetic Medical Products	1989-02-03	11
K890373	HEMORRHOIDAL FORCEPS	Kinetic Medical Products	1989-02-03	11
K890374	ABDOMINAL SPATULA	Kinetic Medical Products	1989-02-03	11
K890381	PARAMETRIUM CLAMP	Kinetic Medical Products	1989-02-03	11
K890211	MICROSURGICAL NEEDLE HOLDERS	Kinetic Medical Products	1989-01-27	9
K890212	MICROSURGICAL SCISSORS	Kinetic Medical Products	1989-01-27	9
K890213	MICROSURGICAL FORCEPS	Kinetic Medical Products	1989-01-27	9
K890214	MICROSURGERY RAZOR BLADE HOLDER	Kinetic Medical Products	1989-01-27	9
K890215	MICROSURGICAL SCARIFIER	Kinetic Medical Products	1989-01-27	9
K890217	MICROSURGICAL KNIVES	Kinetic Medical Products	1989-01-27	9
K890218	MICROSURGICAL CYSTOTOME	Kinetic Medical Products	1989-01-27	9
K890221	MICROSURGICAL WIRE LOOP	Kinetic Medical Products	1989-01-27	9
K890225	SURGICAL SCISSORS	Kinetic Medical Products	1989-01-27	9
K890226	SURGICAL FORCEPS	Kinetic Medical Products	1989-01-27	9
K890227	SURGICAL PROBE	Kinetic Medical Products	1989-01-27	9
K890228	SURGICAL NEEDLE GUIDE	Kinetic Medical Products	1989-01-27	9
K890229	SURGICAL NEEDLE HOLDERS	Kinetic Medical Products	1989-01-27	9
K890230	LIGATURE NEEDLES	Kinetic Medical Products	1989-01-27	9
K890231	SURGICAL TOWEL CLIPS	Kinetic Medical Products	1989-01-27	9
K890233	SUTURE CLIP APPLIER/REMOVER	Kinetic Medical Products	1989-01-27	9
K890234	SUTURE CLIP REMOVER	Kinetic Medical Products	1989-01-27	9
K890238	CATHETER FORCEPS	Kinetic Medical Products	1989-01-27	9
K890242	SCALPEL HANDLE	Kinetic Medical Products	1989-01-27	9
K890243	DRESSING FORCEPS	Kinetic Medical Products	1989-01-27	9
K890244	TUBING CLAMP FORCEPS	Kinetic Medical Products	1989-01-27	9
K890245	SURGICAL HEMOSTATS	Kinetic Medical Products	1989-01-27	9
K890246	ARTERY FORCEPS	Kinetic Medical Products	1989-01-27	9
K890247	SURGICAL RETRACTORS	Kinetic Medical Products	1989-01-27	9
K890248	SURGICAL RETRACTORS	Kinetic Medical Products	1989-01-27	9

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