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-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K932210 | ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT | Dow Corning Wright | 1994-09-07 | 488 | 0 |
| K932911 | ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENT | Dow Corning Wright | 1994-06-30 | 379 | 0 |
| K934354 | LACEY ALL POLYETHYLENE TIBIAL COMPONENT | Dow Corning Wright | 1994-06-03 | 269 | 0 |
| K932222 | SLT FEMORAL HEAD | Dow Corning Wright | 1994-05-27 | 385 | 0 |
| K932858 | ORTHOLOC ADVANTIM TIBIAL BASE COMPONENT | Dow Corning Wright | 1994-02-16 | 251 | 0 |
| K930228 | ORTHOLOC ADVANTIM TIBIAL STEM 5 DEGREE | Dow Corning Wright | 1993-11-30 | 315 | 0 |
| K925900 | LACEY REVISION FEMORAL COMPONENT | Dow Corning Wright | 1993-08-24 | 277 | 0 |
| K930189 | ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMP | Dow Corning Wright | 1993-08-06 | 204 | 0 |
| K930188 | ORTHOLOC(R) ADVANTIM(TM) FEMORAL COMPONENT | Dow Corning Wright | 1993-08-03 | 201 | 0 |
| K930190 | ORTHOLOC(R) ADVANTIM(TM) NON-POR COAT FEMOR COMP | Dow Corning Wright | 1993-08-02 | 200 | 0 |
| K926257 | ORTHOLOC ADVANTIM THICK TIBIAL BASE COMPONENT | Dow Corning Wright | 1993-05-18 | 151 | 0 |
| K915525 | WHITESIDE ORTHOLOC(R) MODULAR REVISION FEMOR COMP | Dow Corning Wright | 1993-05-05 | 512 | 0 |
| K920968 | INFINITY(R) COLLARLESS/MICROTAPER TROCHANTERIC MOD | Dow Corning Wright | 1993-05-05 | 429 | 0 |
| K920969 | HYDROXYLAPATITE INFINITY(R) | Dow Corning Wright | 1993-05-05 | 429 | 0 |
| K920929 | POLY INSERT 20 DEGREE | Dow Corning Wright | 1993-05-05 | 432 | 0 |
| K925512 | CERAMIC FEMORAL HEAD-28MM LONG, MODIFICATION | Dow Corning Wright | 1993-02-12 | 210 | 0 |
| K920593 | CERAMIC FEMORAL HEAD | Dow Corning Wright | 1992-08-31 | 202 | 0 |
| K915448 | CORTICAL BONE SCREW | Dow Corning Wright | 1992-02-28 | 81 | 0 |
| K915238 | TRAC-WRIGHT TRAC 10 CATHETER | Dow Corning Wright | 1992-02-19 | 90 | 0 |
| K915350 | HYDROXYAPATITE INFINITY TROCHANTERIC MODULE | Dow Corning Wright | 1992-02-03 | 69 | 0 |
| K914169 | WHITESIDE ORTHOLOC MOD.TIBIAL AUGMENTATION COMP | Dow Corning Wright | 1992-01-27 | 132 | 0 |
| K913874 | INFINITY(TM) MICROTAPER HIP SYSTEM | Dow Corning Wright | 1991-11-27 | 90 | 0 |
| K913783 | CORDIS PTCA GUIDING CATHETER, MODIFICATION | Dow Corning Wright | 1991-10-18 | 65 | 0 |
| K912452 | HA MCCUTCHEN SLT HIP SYSTEM | Dow Corning Wright | 1991-10-04 | 123 | 0 |
| K910594 | TRAC-WRIGHT SYSTEM, MODEL TW2 | Dow Corning Wright | 1991-09-23 | 223 | 0 |
| K911595 | INFINITY(TM) POROUS-COATED TROCHANTERIC MODULE | Dow Corning Wright | 1991-07-12 | 94 | 0 |
| K911052 | NEXUS(TM) FEMORAL HIP STEM | Dow Corning Wright | 1991-06-17 | 101 | 0 |
| K910596 | DCW MODULAR DISTAL FEMORAL SYSTEM | Dow Corning Wright | 1991-05-29 | 106 | 0 |
| K905408 | NEXUS ACETABULAR CUP | Dow Corning Wright | 1991-03-01 | 88 | 0 |
| K905076 | WHITESIDE ORTHOLOC MODULAR TIBIAL CONSTRAIN.INSERT | Dow Corning Wright | 1991-02-13 | 92 | 0 |
| K904028 | DCW MODULAR PROXIMAL FEMORAL SYSTEM | Dow Corning Wright | 1991-01-14 | 136 | 0 |
| K904680 | THERATEK GROUP EXCHANGE CATHETER | Dow Corning Wright | 1990-12-27 | 73 | 0 |
| K902538 | WHITESIDE ORTHOLOC MODULAR TIBIAL AUGMENTATION | Dow Corning Wright | 1990-07-06 | 30 | 0 |
| K901992 | WHITESIDE ORTHOLOC MODULAR POST. STAB. KNEE SYSTEM | Dow Corning Wright | 1990-06-26 | 55 | 0 |
| K896081 | WHITESIDE ORTHOLOC MODULAR METAL-BACKED PATELLA | Dow Corning Wright | 1990-03-02 | 134 | 0 |
| K896045 | WHITESIDE ORTHOLOC MODULAR-C TOTAL KNEE SYSTEM | Dow Corning Wright | 1990-01-05 | 80 | 0 |
| K894226 | SILASTIC SOFT SHEETING | Dow Corning Wright | 1990-01-03 | 198 | 0 |
| K896105 | EVOLUTION HIP SYSTEM | Dow Corning Wright | 1989-12-29 | 70 | 0 |
| K895399 | KIM MODULAR FEMORAL HIP PROSTHESIS | Dow Corning Wright | 1989-12-14 | 98 | 0 |
| K894965 | POROUS-COATED TITANIUM ACETABULAR CUP | Dow Corning Wright | 1989-11-17 | 102 | 0 |
| K894504 | WHITESIDE ORTHOLOC M.A. TIBIAL BASE | Dow Corning Wright | 1989-10-17 | 90 | 0 |
| K893685 | CERAMIC FEMORAL HEAD | Dow Corning Wright | 1989-09-26 | 133 | 0 |
| K893252 | WHITESIDE ORTHOLOC M.A. TOTAL KNEE SYSTEM | Dow Corning Wright | 1989-07-28 | 91 | 0 |
| K884338 | LACEY POSTERIOR STABILIZED KNEE SYSTEM | Dow Corning Wright | 1989-02-01 | 110 | 0 |
| K884561 | KOENIG TOTAL TOE IMPLANT | Dow Corning Wright | 1989-01-24 | 85 | 0 |
| K881779 | WHITESIDE ORTHOLOC II UNICONDYLAR KNEE SYSTEM | Dow Corning Wright | 1988-08-31 | 127 | 0 |
| K880405 | SILASTIC NASAL IMPLANT S-TYPE | Dow Corning Wright | 1988-02-18 | 20 | 0 |
| K874575 | PROXIMAL FEMORAL REPLACEMENT PROSTHESIS | Dow Corning Wright | 1988-01-07 | 62 | 0 |
| K874740 | WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO | Dow Corning Wright | 1987-12-18 | 30 | 0 |
| K873857 | WHITESIDE ORTHOLOC REVISION HIP STEM PROSTHESIS | Dow Corning Wright | 1987-12-01 | 70 | 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