Integral®
GUDID 00889024010901
ZIMMER DENTAL INC.
Dental implant suprastructure, permanent, preformed| Primary Device ID | 00889024010901 |
| NIH Device Record Key | de5f3a70-4146-4037-988a-8664e5ad4b28 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Integral® |
| Version Model Number | 0422 |
| 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 | 00889024010901 [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 |
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
Moist Heat or Steam Sterilization
[00889024010901]
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®]
| 00889024011434 | 0949 |
| 00889024011427 | 0948 |
| 00889024010918 | 0426 |
| 00889024010901 | 0422 |
| 00889024010956 | 0494 |
| 00889024011465 | 0999 |
| 00889024011403 | 0936 |
| 00889024011373 | 0837 |
| 00889024011359 | 0815 |
| 00889024011151 | 0701 |
| 00889024010925 | 0431 |
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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