Screw-Vent®
GUDID 00889024018273
ZIMMER DENTAL INC.
Screw endosteal dental implant, two-piece| Primary Device ID | 00889024018273 |
| NIH Device Record Key | 6b2750ea-2603-4f4b-be49-4cfa29fae9af |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Screw-Vent® |
| Version Model Number | SVWB16 |
| Company DUNS | 103167086 |
| Company Name | ZIMMER DENTAL INC. |
| Device Count | 1 |
| DM Exempt | false |
| 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 | 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 |
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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024018273 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K011028
FDA Product Code
| DZE | Implant, Endosseous, Root-Form |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-05-31 |
On-Brand Devices [Screw-Vent®]
| 00889024020337 | WT |
| 00889024018358 | T3.3 |
| 00889024018297 | SVWD |
| 00889024018181 | SVMD16 |
| 00889024018174 | SVMD13 |
| 00889024018167 | SVMD10 |
| 00889024018075 | SVDS |
| 00889024017726 | STD3.3 |
| 00889024017719 | STD |
| 00889024018341 | SVWH8 |
| 00889024018334 | SVWH16 |
| 00889024018327 | SVWH13 |
| 00889024018310 | SVWH10 |
| 00889024018273 | SVWB16 |
| 00889024018235 | SVMH8 |
| 00889024018228 | SVMH16 |
| 00889024018211 | SVMH13 |
| 00889024018204 | SVMH10 |
| 00889024018112 | SVH8 |
| 00889024018105 | SVH16 |
| 00889024018099 | SVH13 |
| 00889024018082 | SVH10 |
Trademark Results [Screw-Vent]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SCREW-VENT 73587322 1463379 Live/Registered |
CORE-VENT CORPORATION 1986-03-10 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.