KINCISE 299966809
GUDID 10603295535522
KINCISE V1 MAKE TO ORDER EMPHASYS OFFSET CUP IMPACTOR
DEPUY ORTHOPAEDICS, INC.
Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable| Primary Device ID | 10603295535522 |
| NIH Device Record Key | 6c69cc05-6bc6-41e3-a010-f9769346ee62 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KINCISE |
| Version Model Number | 2999-66-809 |
| Catalog Number | 299966809 |
| Company DUNS | 080506581 |
| Company Name | DEPUY ORTHOPAEDICS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx | |
| Phone | +1(800)255-2500 |
| xx@xx.xx |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10603295535522 [Primary] |
FDA Product Code
| HWE | INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
[10603295535522]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-11-15 |
| Device Publish Date | 2023-11-07 |
On-Brand Devices [KINCISE]
| 10603295511267 | KINCISE MAKE TO ORDER OFFSET CUP IMPACTOR |
| 10603295549246 | KINCISE MAKE TO ORDER DUAL OFFSET BROACH HANDLE MODIFIED SHORT LEFT |
| 10603295549222 | KINCISE MAKE TO ORDER DUAL OFFSET BROACH HANDLE MODIFIED SHORT RIGHT |
| 10603295535614 | KINCISE V1 MAKE TO ORDER EMPHASYS STRAIGHT CUP IMPACTOR |
| 10603295535522 | KINCISE V1 MAKE TO ORDER EMPHASYS OFFSET CUP IMPACTOR |
Trademark Results [KINCISE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 KINCISE 90105877 not registered Live/Pending |
Depuy Synthes, Inc. 2020-08-11 |
 KINCISE 88032292 not registered Live/Pending |
Depuy Synthes, Inc. 2018-07-10 |
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