| Primary Device ID | 07332747211665 |
| NIH Device Record Key | 6f9702b3-1095-481f-97b9-d2ea5d11adcc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Omnigrip™ |
| Version Model Number | 37377 |
| Catalog Number | 37377 |
| Company DUNS | 353939929 |
| Company Name | Nobel Biocare AB |
| 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 | true |
| 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 |
| Phone | +1(800)322-5001 |
| us.customerservice@nobelbiocare.com | |
| Phone | +1(800)322-5001 |
| us.customerservice@nobelbiocare.com | |
| Phone | +1(800)322-5001 |
| us.customerservice@nobelbiocare.com | |
| Phone | +1(800)322-5001 |
| us.customerservice@nobelbiocare.com | |
| Phone | +1(800)322-5001 |
| us.customerservice@nobelbiocare.com | |
| Phone | +1(800)322-5001 |
| us.customerservice@nobelbiocare.com | |
| Phone | +1(800)322-5001 |
| us.customerservice@nobelbiocare.com | |
| Phone | +1(800)322-5001 |
| us.customerservice@nobelbiocare.com | |
| Phone | +1(800)322-5001 |
| us.customerservice@nobelbiocare.com | |
| Phone | +1(800)322-5001 |
| us.customerservice@nobelbiocare.com | |
| Phone | +1(800)322-5001 |
| us.customerservice@nobelbiocare.com | |
| Phone | +1(800)322-5001 |
| us.customerservice@nobelbiocare.com | |
| Phone | +1(800)322-5001 |
| us.customerservice@nobelbiocare.com |
| Length | 28 Millimeter |
| Length | 28 Millimeter |
| Length | 28 Millimeter |
| Length | 28 Millimeter |
| Length | 28 Millimeter |
| Length | 28 Millimeter |
| Length | 28 Millimeter |
| Length | 28 Millimeter |
| Length | 28 Millimeter |
| Length | 28 Millimeter |
| Length | 28 Millimeter |
| Length | 28 Millimeter |
| Length | 28 Millimeter |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight. Keep dry |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07332747211665 [Primary] |
| NDP | Accessories, implant, dental, endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07332747211665]
Moist Heat or Steam Sterilization
[07332747211665]
Moist Heat or Steam Sterilization
[07332747211665]
Moist Heat or Steam Sterilization
[07332747211665]
Moist Heat or Steam Sterilization
[07332747211665]
Moist Heat or Steam Sterilization
[07332747211665]
Moist Heat or Steam Sterilization
[07332747211665]
Moist Heat or Steam Sterilization
[07332747211665]
Moist Heat or Steam Sterilization
[07332747211665]
Moist Heat or Steam Sterilization
[07332747211665]
Moist Heat or Steam Sterilization
[07332747211665]
Moist Heat or Steam Sterilization
[07332747211665]
Moist Heat or Steam Sterilization
[07332747211665]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-07-31 |
| Device Publish Date | 2025-07-23 |
| 07332747085914 | Omnigrip Clinical Screw CC RP/WP |
| 07332747078770 | Omnigrip Clinical Screw CC NP |
| 07332747078763 | Omnigrip Clinical Screw CC RP |
| 07332747175622 | Omnigrip Lab Screw CC RP/WP |
| 07332747078664 | Omnigrip Screwdriver Manual 36mm |
| 07332747078671 | Omnigrip Screwdriver Manual 28mm |
| 07332747078688 | Omnigrip Screwdriver Manual 20mm |
| 07332747175424 | Omnigrip Lab Screw CC RP |
| 07332747175417 | Omnigrip Lab Screw CC NP |
| 07332747078695 | Omnigrip Lab Screw CC RP |
| 07332747078657 | Omnigrip Screwdriver Machine 20mm |
| 07332747078640 | Omnigrip Screwdriver Machine 25mm |
| 07332747078633 | Omnigrip Screwdriver Machine 30mm |
| 07332747078626 | Omnigrip Screwdriver Machine 35mm |
| 07332747201635 | Omnigrip Clinical Screw Titanium Tri-Channel RP/WP/6.0 |
| 07332747201611 | Omnigrip Clinical Screw Titanium Tri-Channel NP |
| 07332747201598 | Omnigrip Clinical Screw Titanium CC RP/WP |
| 07332747201574 | Omnigrip Clinical Screw Titanium CC NP |
| 07332747201642 | Omnigrip Laboratory Screw Titanium Tri-Channel RP/WP/6.0 |
| 07332747201628 | Omnigrip Laboratory Screw Titanium Tri-Channel NP |
| 07332747201604 | Omnigrip Laboratory Screw Titanium CC RP/WP |
| 07332747201581 | Omnigrip Laboratory Screw Titanium CC NP |
| 07332747221824 | Omnigrip Laboratory Screw Titanium Tri-Channel RP/WP/6.0 |
| 07332747221817 | Omnigrip Clinical Screw Titanium Tri-Channel RP/WP/6.0 |
| 07332747221800 | Omnigrip Laboratory Screw Titanium Tri-Channel NP |
| 07332747221794 | Omnigrip Clinical Screw Titanium Tri-Channel NP |
| 07332747221787 | Omnigrip Laboratory Screw Titanium CC RP/WP |
| 07332747221770 | Omnigrip Clinical Screw Titanium CC RP/WP |
| 07332747221763 | Omnigrip Laboratory Screw Titanium CC NP |
| 07332747221756 | Omnigrip Clinical Screw Titanium CC NP |
| 07332747211894 | Omnigrip™ Lab Screw CC RP/WP |
| 07332747211887 | Omnigrip™ Clinical Screw CC RP/WP |
| 07332747211641 | Omnigrip™ Lab Screw CC RP |
| 07332747211634 | Omnigrip™ Lab Screw CC NP |
| 07332747211627 | Omnigrip™ Clinical Screw CC NP |
| 07332747211719 | Omnigrip™ Screwdriver Machine 35mm |
| 07332747211702 | Omnigrip™ Screwdriver Machine 30mm |
| 07332747211696 | Omnigrip™ Screwdriver Machine 25mm |
| 07332747211689 | Omnigrip™ Screwdriver Machine 20mm |
| 07332747211672 | Omnigrip™ Screwdriver Manual 36mm |
| 07332747211665 | Omnigrip™ Screwdriver Manual 28mm |
| 07332747211658 | Omnigrip™ Screwdriver Manual 20mm |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() OMNIGRIP 86732911 5116987 Live/Registered |
CURT Manufacturing, LLC 2015-08-21 |
![]() OMNIGRIP 86616627 4947848 Live/Registered |
Three-Fifteen, Inc. 2015-05-01 |
![]() OMNIGRIP 79041963 3480906 Dead/Cancelled |
ORANGE INTERNATIONAL TRADING (TIANJIN) INC. 2007-06-07 |
![]() OMNIGRIP 76565909 2986938 Live/Registered |
PRYM CONSUMER USA INC. 2003-12-08 |
![]() OMNIGRIP 76360773 2677307 Live/Registered |
CUSTOM BUILDING PRODUCTS, LLC 2002-01-17 |
![]() OMNIGRIP 76302589 not registered Dead/Abandoned |
Albany International Corp. 2001-08-20 |
![]() OMNIGRIP 74009146 not registered Dead/Abandoned |
OMNIGRID, INC. 1989-12-08 |
![]() OMNIGRIP 73101961 1075551 Dead/Expired |
EQUIPMENT INNOVATORS, INC. 1976-10-04 |
![]() OMNIGRIP 73014071 0998939 Dead/Expired |
MINIGRIP, INC. 1974-02-22 |