Integral® Implant System
GUDID 00889024011182
ZIMMER DENTAL INC.
Dental implant suprastructure, permanent, preformed| Primary Device ID | 00889024011182 |
| NIH Device Record Key | 6252c4e7-1e7a-43e8-8d4d-232daaf8cf13 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Integral® Implant System |
| Version Model Number | 0712 |
| Company DUNS | 103167086 |
| Company Name | ZIMMER DENTAL INC. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | 00889024011182 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K900549
FDA Product Code
| DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
Moist Heat or Steam Sterilization
[00889024011182]
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 | 2017-09-15 |
On-Brand Devices [Integral® Implant System]
| 00889024011458 | 0996 |
| 00889024011441 | 0995 |
| 00889024011397 | 0932 |
| 00889024011267 | 0761 |
| 00889024011250 | 0760 |
| 00889024011199 | 0713 |
| 00889024011182 | 0712 |
| 00889024011175 | 0711 |
| 00889024011168 | 0710 |
| 00889024010840 | 0317 |
Trademark Results [Integral]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INTEGRAL 98524557 not registered Live/Pending |
ESSENTIAL HARVEST HEALTH LLC 2024-04-29 |
 INTEGRAL 98469220 not registered Live/Pending |
Essentially Engineered, LLC 2024-03-26 |
 INTEGRAL 98412173 not registered Live/Pending |
Integral Development Corp. 2024-02-20 |
 INTEGRAL 98412171 not registered Live/Pending |
Integral Development Corp. 2024-02-20 |
 INTEGRAL 98358945 not registered Live/Pending |
Integral Energy Services USA Inc. 2024-01-16 |
 INTEGRAL 98342850 not registered Live/Pending |
ÃNSALAN TEXTILE INDUSTRY AND TRADE LIMITED COMPANY 2024-01-04 |
 INTEGRAL 98239396 not registered Live/Pending |
Essentially Engineered, LLC 2023-10-25 |
 INTEGRAL 98000480 not registered Live/Pending |
100th Meridian Ventures, LLC 2023-05-17 |
 INTEGRAL 97686309 not registered Live/Pending |
Integral Development Corp. 2022-11-21 |
 INTEGRAL 97686307 not registered Live/Pending |
Integral Development Corp. 2022-11-21 |
 INTEGRAL 97683411 not registered Live/Pending |
Essentially Engineered, LLC 2022-11-18 |
 INTEGRAL 97412352 not registered Live/Pending |
Essentially Engineered, LLC 2022-05-16 |
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