Dow Corning Wright
Mchenry, IL, US
Dow Corning Wright appears in FDA device records in Mchenry, IL. FDA records list 74 510(k) clearances between and , one PMA record and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 74
- PMA records
- 1
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
Showing 50 of 74FDA records hold 74 510(k) clearances for Dow Corning Wright between 1979 and 1994. The busiest year on record is 1987, with 15. The most recent is 1994, with 5.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1979 | 1 |
| 1980 | 5 |
| 1983 | 1 |
| 1986 | 4 |
| 1987 | 15 |
| 1988 | 3 |
| 1989 | 8 |
| 1990 | 6 |
| 1991 | 10 |
| 1992 | 5 |
| 1993 | 11 |
| 1994 | 5 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K932210 | ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT | JWH | Substantially Equivalent for Some Indications | |
| K932911 | ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENT | JWH | Substantially Equivalent for Some Indications | |
| K934354 | LACEY ALL POLYETHYLENE TIBIAL COMPONENT | JWH | Substantially Equivalent | |
| K932222 | SLT FEMORAL HEAD | LZO | Substantially Equivalent | |
| K932858 | ORTHOLOC ADVANTIM TIBIAL BASE COMPONENT | JWH | Substantially Equivalent | |
| K930228 | ORTHOLOC ADVANTIM TIBIAL STEM 5 DEGREE | JWH | Substantially Equivalent | |
| K925900 | LACEY REVISION FEMORAL COMPONENT | JWH | Substantially Equivalent | |
| K930189 | ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMP | JWH | Substantially Equivalent for Some Indications | |
| K930188 | ORTHOLOC(R) ADVANTIM(TM) FEMORAL COMPONENT | JWH | Substantially Equivalent | |
| K930190 | ORTHOLOC(R) ADVANTIM(TM) NON-POR COAT FEMOR COMP | JWH | Substantially Equivalent | |
| K926257 | ORTHOLOC ADVANTIM THICK TIBIAL BASE COMPONENT | JWH | Substantially Equivalent | |
| K920969 | HYDROXYLAPATITE INFINITY(R) | MEH | Substantially Equivalent | |
| K920968 | INFINITY(R) COLLARLESS/MICROTAPER TROCHANTERIC MOD | LZO | Substantially Equivalent | |
| K920929 | POLY INSERT 20 DEGREE | JDL | Substantially Equivalent | |
| K915525 | WHITESIDE ORTHOLOC(R) MODULAR REVISION FEMOR COMP | JWH | Substantially Equivalent | |
| K925512 | CERAMIC FEMORAL HEAD-28MM LONG, MODIFICATION | LZO | Substantially Equivalent | |
| K920593 | CERAMIC FEMORAL HEAD | LZO | Substantially Equivalent | |
| K915448 | CORTICAL BONE SCREW | HWC | Substantially Equivalent | |
| K915238 | TRAC-WRIGHT TRAC 10 CATHETER | MCW | Substantially Equivalent | |
| K915350 | HYDROXYAPATITE INFINITY TROCHANTERIC MODULE | MEH | Substantially Equivalent | |
| K914169 | WHITESIDE ORTHOLOC MOD.TIBIAL AUGMENTATION COMP | JWH | Substantially Equivalent | |
| K913874 | INFINITY(TM) MICROTAPER HIP SYSTEM | JDI | Substantially Equivalent | |
| K913783 | CORDIS PTCA GUIDING CATHETER, MODIFICATION | DQY | Substantially Equivalent | |
| K912452 | HA MCCUTCHEN SLT HIP SYSTEM | MEH | Substantially Equivalent | |
| K910594 | TRAC-WRIGHT SYSTEM, MODEL TW2 | DXT | Substantially Equivalent | |
| K911595 | INFINITY(TM) POROUS-COATED TROCHANTERIC MODULE | JDG | Substantially Equivalent for Some Indications | |
| K911052 | NEXUS(TM) FEMORAL HIP STEM | JDI | Substantially Equivalent | |
| K910596 | DCW MODULAR DISTAL FEMORAL SYSTEM | KRO | Substantially Equivalent | |
| K905408 | NEXUS ACETABULAR CUP | JDI | Substantially Equivalent | |
| K905076 | WHITESIDE ORTHOLOC MODULAR TIBIAL CONSTRAIN.INSERT | JWH | Substantially Equivalent | |
| K904028 | DCW MODULAR PROXIMAL FEMORAL SYSTEM | LZO | Substantially Equivalent for Some Indications | |
| K904680 | THERATEK GROUP EXCHANGE CATHETER | MCW | Substantially Equivalent | |
| K902538 | WHITESIDE ORTHOLOC MODULAR TIBIAL AUGMENTATION | HRY | Substantially Equivalent for Some Indications | |
| K901992 | WHITESIDE ORTHOLOC MODULAR POST. STAB. KNEE SYSTEM | JWH | Substantially Equivalent for Some Indications | |
| K896081 | WHITESIDE ORTHOLOC MODULAR METAL-BACKED PATELLA | JWH | Substantially Equivalent for Some Indications | |
| K896045 | WHITESIDE ORTHOLOC MODULAR-C TOTAL KNEE SYSTEM | JWH | Substantially Equivalent for Some Indications | |
| K894226 | SILASTIC SOFT SHEETING | FRO | Substantially Equivalent | |
| K896105 | EVOLUTION HIP SYSTEM | KWL | Substantially Equivalent for Some Indications | |
| K895399 | KIM MODULAR FEMORAL HIP PROSTHESIS | LZO | Substantially Equivalent | |
| K894965 | POROUS-COATED TITANIUM ACETABULAR CUP | JDL | Substantially Equivalent for Some Indications | |
| K894504 | WHITESIDE ORTHOLOC M.A. TIBIAL BASE | JWH | Substantially Equivalent | |
| K893685 | CERAMIC FEMORAL HEAD | LZO | Substantially Equivalent | |
| K893252 | WHITESIDE ORTHOLOC M.A. TOTAL KNEE SYSTEM | JWH | Substantially Equivalent for Some Indications | |
| K884338 | LACEY POSTERIOR STABILIZED KNEE SYSTEM | JWH | Substantially Equivalent for Some Indications | |
| K884561 | KOENIG TOTAL TOE IMPLANT | LZJ | Substantially Equivalent for Some Indications | |
| K881779 | WHITESIDE ORTHOLOC II UNICONDYLAR KNEE SYSTEM | HSX | Substantially Equivalent for Some Indications | |
| K880405 | SILASTIC NASAL IMPLANT S-TYPE | FZE | Substantially Equivalent | |
| K874575 | PROXIMAL FEMORAL REPLACEMENT PROSTHESIS | JDG | Substantially Equivalent | |
| K874740 | WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO | JDG | Substantially Equivalent for Some Indications | |
| K873857 | WHITESIDE ORTHOLOC REVISION HIP STEM PROSTHESIS | JDI | Substantially Equivalent for Some Indications |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- DQYCatheter, Percutaneous
- MCWCatheter, Peripheral, Atherectomy
- JSGCulture Media, Non-Selective And Non-Differential
- FRODressing, Wound, Drug
- DXTInjector And Syringe, Angiographic
- LXHOrthopedic Manual Surgical Instrument
- IPYOrthosis, Lumbo-Sacral
- JDGProsthesis, Hip, Femoral Component, Cemented, Metal
- KWLProsthesis, Hip, Hemi-, Femoral, Metal
- KWYProsthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
- JDLProsthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)
- LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
- JDIProsthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
- LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- MEHProsthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
- KROProsthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
- HSXProsthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
- HRYProsthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
- JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
- FZEProsthesis, Nose, Internal
- LZJProsthesis, Toe (Metatarsophalangeal), Joint, Metal/Polymer, Semi-Constrained
- KWDProsthesis, Toe, Hemi-, Phalangeal
- KWNProsthesis, Wrist, Carpal Lunate
- KWOProsthesis, Wrist, Carpal Scaphoid
- KYIProsthesis, Wrist, Carpal Trapezium
- KWMProsthesis, Wrist, Semi-Constrained
- GZTRetractor, Self-Retaining, For Neurosurgery
- HWCScrew, Fixation, Bone
- GZJStimulator, Nerve, Transcutaneous, For Pain Relief
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain