Magicore
GUDID 08800039354929
InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)
Dental implant system| Primary Device ID | 08800039354929 |
| NIH Device Record Key | 2497e6fb-529b-428d-8726-fb5e7851971b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Magicore |
| Version Model Number | 452M5009 |
| Company DUNS | 631169224 |
| Company Name | InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd) |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08800039354929 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K201981
FDA Product Code
| DZE | Implant, Endosseous, Root-Form |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-09-08 |
| Device Publish Date | 2020-08-31 |
On-Brand Devices [Magicore]
Trademark Results [Magicore]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MAGICORE 97074352 not registered Live/Pending |
Common Core Kingdom, LLC 2021-10-14 |
 MAGICORE 78346009 not registered Dead/Abandoned |
Bayer Polymers LLC 2003-12-29 |
 MAGICORE 78092721 2856704 Dead/Cancelled |
BAYER MATERIALSCIENCE LLC 2001-11-12 |
 MAGICORE 76182998 not registered Dead/Abandoned |
Advanced Lighting Technologies, Inc. 2000-12-19 |
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