Swish™ Duo-Grip™ Healing Collar 9065-12H
GUDID 10841307115892
IMPLANT DIRECT SYBRON MANUFACTURING LLC
Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed| Primary Device ID | 10841307115892 |
| NIH Device Record Key | ada4410d-85a9-4002-b317-338452f5d69a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Swish™ Duo-Grip™ Healing Collar |
| Version Model Number | 9065-12H |
| Catalog Number | 9065-12H |
| Company DUNS | 868856969 |
| Company Name | IMPLANT DIRECT SYBRON MANUFACTURING LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10841307115892 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K090234
FDA Product Code
| NHA | Abutment, Implant, Dental, Endosseous |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2015-09-14 |
On-Brand Devices [Swish™ Duo-Grip™ Healing Collar]
| 10841307115922 | 9065-15H |
| 10841307115915 | 9065-14H |
| 10841307115908 | 9065-13H |
| 10841307115892 | 9065-12H |
| 10841307115885 | 9048-15H |
| 10841307115878 | 9048-14H |
| 10841307115861 | 9048-13H |
| 10841307115854 | 9048-12H |
| 10841307115847 | 9037-15H |
| 10841307115830 | 9037-14H |
| 10841307115823 | 9037-13H |
| 10841307115816 | 9037-12H |
| 10841307130260 | 9065-13H |
| 10841307130253 | 9048-13H |
| 10841307130246 | 9037-13H |
Trademark Results [Swish]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SWISH 98177975 not registered Live/Pending |
Swish Bio, LP 2023-09-13 |
 SWISH 97676287 not registered Live/Pending |
InMobi Pte Ltd. 2022-11-14 |
 SWISH 97539021 not registered Live/Pending |
Waggoner Medical Consulting, PLLC 2022-08-08 |
 SWISH 97508676 not registered Live/Pending |
NORTHBOUND FILMS, INC 2022-07-18 |
 SWISH 97332259 not registered Live/Pending |
The Breeze Drinks Company Ltd. 2022-03-26 |
 SWISH 97092870 not registered Live/Pending |
DeepCoding Ltd. 2021-10-26 |
 SWISH 90857730 not registered Live/Pending |
Colgate-Palmolive Company 2021-07-30 |
 SWISH 90845148 not registered Live/Pending |
Harrell and Earnhart Collaborative, LLC 2021-07-23 |
 SWISH 90692847 not registered Live/Pending |
Swish Equestrian Ltd 2021-05-06 |
 SWISH 90649182 not registered Live/Pending |
Smile Makers LLC 2021-04-15 |
 SWISH 90511595 not registered Live/Pending |
Daniella Rand 2021-02-04 |
 SWISH 90510506 not registered Live/Pending |
Daniella Rand 2021-02-04 |
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