This page includes the latest FDA filings for Kalitec Medical. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3009165919 |
| FEI Number | 3009165919 |
| Name | Kalitec Direct LLC DBA Kalitec Medical |
| Owner & Operator | Kalitec Medical |
| Contact Address | 865 Oviedo Blvd Suite 1017 Oviedo FL 32765 US |
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 865 Oviedo Blvd Suite 1017 Oviedo, FL 32765 US |
| Establishment Type |
|
Device Company | Device | Date |
|---|---|---|
Kalitec Direct LLC DBA Kalitec Medical [Kalitec Medical] | Kalitec Disc Prep 3 mm Up Biting Pituitary | 2019-12-27 |
Kalitec Direct LLC DBA Kalitec Medical [Kalitec Medical] | Kalitec Disc Prep 3 mm Straight Pituitary | 2019-12-27 |
Kalitec Direct LLC DBA Kalitec Medical [Kalitec Medical] | CosmoLock Pedicle Screw System | 2018-06-20 |
Kalitec Direct LLC DBA Kalitec Medical [Kalitec Medical] | Matira Anterior Cervical System | 2018-06-20 |
Kalitec Direct LLC DBA Kalitec Medical [Kalitec Medical] | TiWAVE L Lumber Trial, 25 x 14mm, 0 Deg, NT STR | 2018-06-20 |
Kalitec Direct LLC DBA Kalitec Medical [Kalitec Medical] | TiWAVE L Lumber Trial, 22 x 16mm, 0 Deg, NT STR | 2018-06-20 |
Kalitec Direct LLC DBA Kalitec Medical [Kalitec Medical] | Ocata Anterior Cervical System | 2017-07-18 |
Kalitec Direct LLC DBA Kalitec Medical [Kalitec Medical] | InSePtion MIS Fixation System | 2017-03-21 |