SwissPlus®
GUDID 00889024020320
ZIMMER DENTAL INC.
Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use| Primary Device ID | 00889024020320 |
| NIH Device Record Key | 0301597d-e429-4ce6-8930-213fc438746e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SwissPlus® |
| Version Model Number | WSX |
| 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 | false |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024020320 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K011038
FDA Product Code
| DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
[00889024020320]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-12-07 |
| Device Publish Date | 2015-10-21 |
On-Brand Devices [SwissPlus®]
| 00889024017559 | SPSCS |
| 00889024017542 | SPSCL |
| 00889024017535 | SPSC |
| 00889024017443 | SPMA2 |
| 00889024017412 | SPGA |
| 00889024016071 | OPWSCL |
| 00889024016064 | OPWSC |
| 00889024015999 | OPSCS |
| 00889024015982 | OPSCL |
| 00889024015975 | OPSC |
| 00889024015944 | OPH20S |
| 00889024015937 | OPH20 |
| 00889024015920 | OPGC |
| 00889024015913 | OPGA |
| 00889024015845 | OPBA3 |
| 00889024015838 | OPBA |
| 00889024015784 | OPAS |
| 00889024015760 | OPACT3 |
| 00889024015753 | OPACT |
| 00889024015722 | OPA2 |
| 00889024015715 | OPA |
| 00889024014947 | GPCAS |
| 00889024020320 | WSX |
| 00889024017528 | SPMT |
| 00889024017450 | SPMAR |
| 00889024016095 | OTL3.0-S |
| 00889024016088 | OT3.0-S |
| 00889024016057 | OPWB8 |
| 00889024016040 | OPWB14 |
| 00889024016033 | OPWB12 |
| 00889024016026 | OPWB10 |
| 00889024016019 | OPT/5 |
| 00889024015968 | OPS |
| 00889024015883 | OPCC |
| 00889024015876 | OPC |
| 00889024015869 | OPBAT |
| 00889024015821 | OPB8 |
| 00889024015814 | OPB14 |
| 00889024015807 | OPB12 |
| 00889024015791 | OPB10 |
| 00889024015746 | OPA/6 |
| 00889024015739 | OPA/5 |
| 00889024015272 | HLRTX2 |
| 00889024014923 | FMTM2 |
| 00889024014886 | FMSW |
| 00889024014879 | FMSM |
| 00889024014862 | FMS |
Trademark Results [SwissPlus]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SWISSPLUS 75908000 2791712 Live/Registered |
ZIMMER DENTAL INC. 2000-02-01 |
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