Swish™ Overdenture Abutment 9048-63
GUDID 10841307116332
IMPLANT DIRECT SYBRON MANUFACTURING LLC
Dental implant suprastructure, permanent, preformed| Primary Device ID | 10841307116332 |
| NIH Device Record Key | eb6bf239-d42e-44a5-a1e8-d05c4b814ef9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Swish™ Overdenture Abutment |
| Version Model Number | 9048-63 |
| Catalog Number | 9048-63 |
| 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 | true |
| Device Combination Product | false |
| Single Use | true |
| 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 | 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 | 10841307116332 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K081396
FDA Product Code
| NHA | Abutment, Implant, Dental, Endosseous |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
[10841307116332]
Moist Heat or Steam Sterilization
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™ Overdenture Abutment]
| 10841307116349 | 9048-64 |
| 10841307116332 | 9048-63 |
| 10841307116325 | 9048-62 |
| 10841307116318 | 9048-61 |
| 10841307116301 | 9037-65 |
| 10841307116295 | 9037-64 |
| 10841307116288 | 9037-63 |
| 10841307116271 | 9037-62 |
| 10841307116264 | 9037-61 |
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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