Dual-Grip™ Extra Short Fixation Screw (2 pieces) 1000-32S
GUDID 10841307108962
IMPLANT DIRECT SYBRON MANUFACTURING LLC
Dental implant suprastructure, permanent, preformed| Primary Device ID | 10841307108962 |
| NIH Device Record Key | 0ab2cac6-f03c-4004-b1f6-fc6c8caf9a3f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Dual-Grip™ Extra Short Fixation Screw (2 pieces) |
| Version Model Number | 1000-32S |
| Catalog Number | 1000-32S |
| Company DUNS | 868856969 |
| Company Name | IMPLANT DIRECT SYBRON MANUFACTURING LLC |
| Device Count | 2 |
| 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 | 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 | 00841307108965 [Unit of Use] |
| GS1 | 10841307108962 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K130572
FDA Product Code
| NHA | Abutment, Implant, Dental, Endosseous |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
Moist Heat or Steam Sterilization
[10841307108962]
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 [Dual-Grip™ Extra Short Fixation Screw (2 pieces)]
| 10841307108993 | 1000-34S |
| 10841307108962 | 1000-32S |
Trademark Results [Dual-Grip]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 DUAL-GRIP 90241709 not registered Live/Pending |
Power Stop LLC 2020-10-08 |
 DUAL-GRIP 85117881 3954407 Live/Registered |
Sofa Mart, LLC 2010-08-27 |
 DUAL-GRIP 78522795 3252310 Live/Registered |
CONTITECH USA, INC. 2004-11-24 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.