This page includes the latest FDA filings for Iotron Industries Usa Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3009504230 |
| FEI Number | 3009504230 |
| Name | IOTRON INDUSTRIES USA INC. |
| Owner & Operator | Iotron Industries USA Inc. |
| Contact Address | 4394 East Park 30 Drive Columbia City IN 46725 US |
| Registration Status | 1 |
| Initial Importer | Y |
| Registration Expiration | 2020-04-25 |
| Registration Address | 4394 East Park 30 Drive Columbia City, IN 46725 US |
| Establishment Type | Sterilize Medical Device for Another Party (Contract Sterilizer) |
Device Company | Device | Date |
|---|---|---|
IOTRON INDUSTRIES USA INC. | Biodesign Staple Line Reinforcement | 2017-08-15 |
IOTRON INDUSTRIES USA INC. | Biodesign Staple Line Reinforcement | 2017-08-15 |
IOTRON INDUSTRIES USA INC. | RSH Biliary Stone Removal Device | 2017-02-06 |
IOTRON INDUSTRIES USA INC. | RSH Biliary Stone Removal Device | 2017-02-06 |
IOTRON INDUSTRIES USA INC. | Nanovis Intervertebral Body Fusion | 2015-11-02 |
IOTRON INDUSTRIES USA INC. | Nanovis Intervertebral Body Fusion | 2015-11-02 |
IOTRON INDUSTRIES USA INC. | Pyng FAST1 | 2012-12-06 |
| NCAGE Code | 7WM98 | IOTRON INDUSTRIES USA INC. |
| CAGE Code | 7WM98 | IOTRON INDUSTRIES USA INC. |
| S.A.M. Registration | 7WM98 [967745204] | IOTRON INDUSTRIES USA INC. |