Tri-Grip™ Fixation Screw Large Diameter 1000-52
GUDID 00841307129779
IMPLANT DIRECT SYBRON MANUFACTURING LLC
Dental implant suprastructure, permanent, preformed| Primary Device ID | 00841307129779 |
| NIH Device Record Key | 99ed3d64-bdec-448f-b5dd-aaafb7819e60 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tri-Grip™ Fixation Screw Large Diameter |
| Version Model Number | 1000-52 |
| Catalog Number | 1000-52 |
| 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
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com | |
| Phone | 1-888-649-6425 |
| customerservice@implantdirect.com |
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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841307129779 [Unit of Use] |
| GS1 | 10841307129776 [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 |
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
[00841307129779]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-03-20 |
| Device Publish Date | 2024-03-12 |
Devices Manufactured by IMPLANT DIRECT SYBRON MANUFACTURING LLC
| 10841307111627 - Legacy™ Plastic Engaging Temporary Abutment | 2024-12-23 |
| 10841307111634 - Legacy™ Plastic Engaging Temporary Abutment | 2024-12-23 |
| 10841307111641 - Legacy™ Plastic Engaging Temporary Abutment | 2024-12-23 |
| 10841307111696 - Legacy™ Plastic Temporary Abutment | 2024-12-23 |
| 10841307103585 - ReActive® Implant | 2024-12-20 Ø3.7 x 8 Platform 3.5mmD |
| 10841307103592 - ReActive® Implant | 2024-12-20 Ø3.7 x 8 Platform 3.5mmD |
| 10841307103608 - ReActive® Implant | 2024-12-20 Ø3.7 x 8 Platform 3.5mmD |
| 10841307103615 - ReActive® Implant | 2024-12-20 Ø3.7 x 8 Platform 3.5mmD |
Trademark Results [Tri-Grip]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 TRI-GRIP 87490432 not registered Live/Pending |
Cello Plastic Products Private Ltd 2017-06-15 |
 TRI-GRIP 87447637 5421979 Live/Registered |
Lexair, Inc. 2017-05-12 |
 TRI-GRIP 86146958 4571959 Live/Registered |
10Back, LLC 2013-12-18 |
 TRI-GRIP 77472778 3649594 Live/Registered |
TASCO CORPORATION 2008-05-13 |
 TRI-GRIP 76643128 3111060 Live/Registered |
Eckel Manufacturing Company, Inc. 2005-07-18 |
 TRI-GRIP 76619393 not registered Dead/Abandoned |
CRI 2000, L.P. 2004-11-03 |
 TRI-GRIP 75327414 not registered Dead/Abandoned |
Collins, Stuart 1997-07-21 |
 TRI-GRIP 74476242 not registered Dead/Abandoned |
Itoya of America, Ltd. 1994-01-04 |
 TRI-GRIP 74420370 1847589 Dead/Cancelled |
GREENLEE TOOLS, INC. 1993-08-04 |
 TRI-GRIP 73828850 1596593 Dead/Cancelled |
ANDERSEN BROTHERS HOLDING COMPANY, INC., THE 1989-10-02 |
 TRI-GRIP 73081225 1048419 Dead/Cancelled |
W. W. Patterson Company 0000-00-00 |
 TRI-GRIP 72110469 0734073 Dead/Expired |
J. R. RICHARDS COMPANY 1960-12-19 |
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