Preat 9000363
GUDID 00842092182208
ASC Zimmer® TSV-compatible 5.7mm Engaging Titanium Base
Preat Corporation
Dental implant suprastructure, temporary, preformed, single-use| Primary Device ID | 00842092182208 |
| NIH Device Record Key | fd4ba815-c5c9-48e3-95fa-7f4d29e78d36 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Preat |
| Version Model Number | 9000363 |
| Catalog Number | 9000363 |
| Company DUNS | 117776048 |
| Company Name | Preat Corporation |
| 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 | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com | |
| Phone | +1(800) 232-7732 |
| info@preat.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00842092182208 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K183518
FDA Product Code
| NHA | Abutment, implant, dental, endosseous |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
[00842092182208]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-04-17 |
| Device Publish Date | 2024-04-09 |
On-Brand Devices [Preat]
| 00842092178102 | Multi-Unit Scan Body w/ .048 Screw Kit Contains:. 1 Multi-Unit Scan Body 1 Multi-Unit Titanium |
| 00842092181577 | BioHorizons®-compatible 4.5mm Clix Complete Ball Abutment 2mm Kit Contains: 1 Clix Ball Abutmen |
| 00842092181553 | O-Ring Mini Implant Servicing Kit Kit contains 2 O-Ring Black Rings #2 Micro Single 1 O-Ring Y |
| 00842092181867 | Straumann Tissue Level WN Analog |
| 00842092182246 | NobelBiocare™ Tri-Lobe-compatible 6.0mm Non-Engaging Verification Cylinder |
| 00842092182239 | NobelBiocare™ Tri-Lobe-compatible 6.0mm Engaging Verification Cylinder |
| 00842092182222 | ASC Biomet 3i Certain®-compatible 3.4mm Non-Engaging Titanium Base |
| 00842092182215 | ASC Zimmer® TSV WP Non-Engaging Titanium Base |
| 00842092182208 | ASC Zimmer® TSV-compatible 5.7mm Engaging Titanium Base |
| 00842092182437 | Multi-Unit Scan Body with Neo Screw |
| 00842092182420 | Multi-Unit Slim Ti Tall Base with Neo Screw |
| 00842092182413 | Multi-Unit Ti Base with Neo Screw |
| 00842092182406 | Multi-Unit Verification Cylinder w/ Neo Screw (100-Pack) |
| 00842092182390 | Multi-Unit Verification Cylinder w/ Neo Screw (50-Pack) |
| 00842092182383 | Multi-Unit Verification Cylinder w/ Neo Screw (10-Pack) |
| 00842092182376 | Multi-Unit Verification Cylinder w/Neo Screw |
| 00842092182369 | Multi-Unit Screw (Neo) (10-Pack) |
| 00842092182352 | Multi-Unit Screw (Neo) |
Trademark Results [Preat]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PREAT 97185837 not registered Live/Pending |
Preat Corporation 2021-12-22 |
 PREAT 97185823 not registered Live/Pending |
Preat Corporation 2021-12-22 |
 PREAT 72269304 0849584 Dead/Expired |
FAULTLESS STARCH COMPANY 1967-04-17 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.