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

Ferguson Medical · Predicate Candidate Screening

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

131 daysmedian FDA review time

542 days90th percentile

57clearances measured

K-number	Device	Applicant	Decided	Review days
K033153	DICOM THEATER	Ferguson Medical	2004-04-23	206
K963794	PUNCTURENEEDLE	Ferguson Medical	1998-03-19	545
K962615	TUMORLOCALIZER MRI	Ferguson Medical	1998-03-19	624
K971813	EMBLA	Ferguson Medical	1998-01-16	245
K972217	ORTHOPEDIC SCREW SYSTEM	Ferguson Medical	1997-11-20	161
K972219	ORTHOPEDIC PLATE SYSTEM	Ferguson Medical	1997-11-20	161
K970819	TARGOBEAM	Ferguson Medical	1997-07-14	131
K970257	FIXANO D.S.S. (DOUBLE SLIDING SCREWS) SYSTEM FOR OSTEOSYNTHE	Ferguson Medical	1997-05-22	119
K970280	FIXANO D.S.S. (DOUBLE SLIDING SCREWS) SYSTEM FOR OSTEOSYNTHE	Ferguson Medical	1997-05-22	119
K970258	FIXANO D.S.S. (DOUBLE SLIDING SCREWS) SYSTEM FOR OSTEOSYNTHS	Ferguson Medical	1997-05-22	119
K960421	SINUSCAN 102/SINUSPRINT	Ferguson Medical	1997-04-16	443
K963894	SMARTGUIDE	Ferguson Medical	1997-03-11	165
K964094	MINIFIX	Ferguson Medical	1996-11-27	47
K964087	BLOCK STOP WIRES	Ferguson Medical	1996-11-25	45
K954772	QUICKELS QS 200 SYSTEM	Ferguson Medical	1996-07-11	272
K954773	QUICKELS QS 100 SYSTEM	Ferguson Medical	1996-07-11	272
K961185	DAUM BIOPSYNEEDLE	Ferguson Medical	1996-04-30	35
K954757	FIXANO D.D.S. (DOUBLE SLIDING SCREW)	Ferguson Medical	1996-01-25	101
K954756	FIXANO I.F.O (INTERLOCKING FLEXIBLE OSTEOSYNTHESIS) SYSTEM	Ferguson Medical	1996-01-25	101
K931265	FIXANO TOTAL TRAPEZIO METACARPAL PROSTHESIS, 2ND	Ferguson Medical	1995-05-22	805
K925732	ISOFLUX IXZ FLOW REGULATOR	Ferguson Medical	1994-05-09	542
K925731	ISOFLUX IXP FLOW REGULATOR	Ferguson Medical	1994-05-09	542
K925733	ISOFLUX IXL FLOW REGULATOR	Ferguson Medical	1994-05-09	542
K925033	STILLE AUTOMATIC TOURNIQUET	Ferguson Medical	1993-02-01	119
K913097	SAM ST	Ferguson Medical	1992-12-11	518
K913095	SAM LS	Ferguson Medical	1992-12-03	510
K913096	SAM SC	Ferguson Medical	1992-12-03	510
K911192	DP 100	Ferguson Medical	1991-12-11	268
K904924	INFUSA PU SYRINGE INFUSION PUMP	Ferguson Medical	1991-09-10	314
K904923	INFUSA T SYRINGE INFUSION PUMP	Ferguson Medical	1991-09-06	310
K904922	INFUSA D.SLT SYRINGE INFUSION PUMP	Ferguson Medical	1991-09-04	308
K904925	INFUSA TS SYRINGE INFUSION PUMP	Ferguson Medical	1991-09-04	308
K901953	AIROX AXR. 1A	Ferguson Medical	1991-01-02	246
K902545	VAAKA BABY SCALE	Ferguson Medical	1990-07-26	48
K890284	URODEC 500	Ferguson Medical	1989-05-30	131
K882413	SUBOCCIPITAL ICE PILLOW	Ferguson Medical	1988-11-30	170
K883133	HANGER, INTRAVENOUS/I.V. BAG HANGER OR HOLDER	Ferguson Medical	1988-11-21	118
K881079	UVP VOLUMED 2001	Ferguson Medical	1988-10-25	225
K882903	YESNG SUPER FRECATOR	Ferguson Medical	1988-07-28	16
K881081	DERMAPOINTS MODEL 200 THERAPEUTIC MASSAGER	Ferguson Medical	1988-07-21	129
K881080	DERMAPOINTS MODEL 100 THERAPEUTIC MASSAGER	Ferguson Medical	1988-07-21	129
K881149	MUCUS TRAP OR SUCTION TRAP	Ferguson Medical	1988-06-14	89
K881407	YESNG RESUABLE BIPOLAR FORCEPS	Ferguson Medical	1988-04-14	10
K881408	YESNG REUSABLE ELECTROSURGICAL HANDLE	Ferguson Medical	1988-04-14	10
K881406	YESNG REUSABLE ELECTROSURGICAL ELECTRODE	Ferguson Medical	1988-04-14	10
K881144	YESNG PATIENT PLATE #80226	Ferguson Medical	1988-04-08	22
K880537	POLE, INTRAVENOUS	Ferguson Medical	1988-04-06	57
K880073	YESNG MODEL 500SII ELECTROSURGICAL UNIT	Ferguson Medical	1988-03-11	60
K880064	YESNG MODEL 200S11 ELECTROSURGICAL UNIT	Ferguson Medical	1988-03-11	64
K880539	CART, MULTIPURPOSE	Ferguson Medical	1988-02-24	15

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