Atlas FDA

Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account

Dow Corning Wright — Predicate Candidate Screening

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

101 daysmedian FDA review time
315 days90th percentile
74clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K932210ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENTDow Corning Wright1994-09-074880
K932911ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENTDow Corning Wright1994-06-303790
K934354LACEY ALL POLYETHYLENE TIBIAL COMPONENTDow Corning Wright1994-06-032690
K932222SLT FEMORAL HEADDow Corning Wright1994-05-273850
K932858ORTHOLOC ADVANTIM TIBIAL BASE COMPONENTDow Corning Wright1994-02-162510
K930228ORTHOLOC ADVANTIM TIBIAL STEM 5 DEGREEDow Corning Wright1993-11-303150
K925900LACEY REVISION FEMORAL COMPONENTDow Corning Wright1993-08-242770
K930189ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMPDow Corning Wright1993-08-062040
K930188ORTHOLOC(R) ADVANTIM(TM) FEMORAL COMPONENTDow Corning Wright1993-08-032010
K930190ORTHOLOC(R) ADVANTIM(TM) NON-POR COAT FEMOR COMPDow Corning Wright1993-08-022000
K926257ORTHOLOC ADVANTIM THICK TIBIAL BASE COMPONENTDow Corning Wright1993-05-181510
K915525WHITESIDE ORTHOLOC(R) MODULAR REVISION FEMOR COMPDow Corning Wright1993-05-055120
K920968INFINITY(R) COLLARLESS/MICROTAPER TROCHANTERIC MODDow Corning Wright1993-05-054290
K920969HYDROXYLAPATITE INFINITY(R)Dow Corning Wright1993-05-054290
K920929POLY INSERT 20 DEGREEDow Corning Wright1993-05-054320
K925512CERAMIC FEMORAL HEAD-28MM LONG, MODIFICATIONDow Corning Wright1993-02-122100
K920593CERAMIC FEMORAL HEADDow Corning Wright1992-08-312020
K915448CORTICAL BONE SCREWDow Corning Wright1992-02-28810
K915238TRAC-WRIGHT TRAC 10 CATHETERDow Corning Wright1992-02-19900
K915350HYDROXYAPATITE INFINITY TROCHANTERIC MODULEDow Corning Wright1992-02-03690
K914169WHITESIDE ORTHOLOC MOD.TIBIAL AUGMENTATION COMPDow Corning Wright1992-01-271320
K913874INFINITY(TM) MICROTAPER HIP SYSTEMDow Corning Wright1991-11-27900
K913783CORDIS PTCA GUIDING CATHETER, MODIFICATIONDow Corning Wright1991-10-18650
K912452HA MCCUTCHEN SLT HIP SYSTEMDow Corning Wright1991-10-041230
K910594TRAC-WRIGHT SYSTEM, MODEL TW2Dow Corning Wright1991-09-232230
K911595INFINITY(TM) POROUS-COATED TROCHANTERIC MODULEDow Corning Wright1991-07-12940
K911052NEXUS(TM) FEMORAL HIP STEMDow Corning Wright1991-06-171010
K910596DCW MODULAR DISTAL FEMORAL SYSTEMDow Corning Wright1991-05-291060
K905408NEXUS ACETABULAR CUPDow Corning Wright1991-03-01880
K905076WHITESIDE ORTHOLOC MODULAR TIBIAL CONSTRAIN.INSERTDow Corning Wright1991-02-13920
K904028DCW MODULAR PROXIMAL FEMORAL SYSTEMDow Corning Wright1991-01-141360
K904680THERATEK GROUP EXCHANGE CATHETERDow Corning Wright1990-12-27730
K902538WHITESIDE ORTHOLOC MODULAR TIBIAL AUGMENTATIONDow Corning Wright1990-07-06300
K901992WHITESIDE ORTHOLOC MODULAR POST. STAB. KNEE SYSTEMDow Corning Wright1990-06-26550
K896081WHITESIDE ORTHOLOC MODULAR METAL-BACKED PATELLADow Corning Wright1990-03-021340
K896045WHITESIDE ORTHOLOC MODULAR-C TOTAL KNEE SYSTEMDow Corning Wright1990-01-05800
K894226SILASTIC SOFT SHEETINGDow Corning Wright1990-01-031980
K896105EVOLUTION HIP SYSTEMDow Corning Wright1989-12-29700
K895399KIM MODULAR FEMORAL HIP PROSTHESISDow Corning Wright1989-12-14980
K894965POROUS-COATED TITANIUM ACETABULAR CUPDow Corning Wright1989-11-171020
K894504WHITESIDE ORTHOLOC M.A. TIBIAL BASEDow Corning Wright1989-10-17900
K893685CERAMIC FEMORAL HEADDow Corning Wright1989-09-261330
K893252WHITESIDE ORTHOLOC M.A. TOTAL KNEE SYSTEMDow Corning Wright1989-07-28910
K884338LACEY POSTERIOR STABILIZED KNEE SYSTEMDow Corning Wright1989-02-011100
K884561KOENIG TOTAL TOE IMPLANTDow Corning Wright1989-01-24850
K881779WHITESIDE ORTHOLOC II UNICONDYLAR KNEE SYSTEMDow Corning Wright1988-08-311270
K880405SILASTIC NASAL IMPLANT S-TYPEDow Corning Wright1988-02-18200
K874575PROXIMAL FEMORAL REPLACEMENT PROSTHESISDow Corning Wright1988-01-07620
K874740WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRODow Corning Wright1987-12-18300
K873857WHITESIDE ORTHOLOC REVISION HIP STEM PROSTHESISDow Corning Wright1987-12-01700

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