This page includes the latest FDA filings for Mai Genesis. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3003697955 |
| FEI Number | 3003697955 |
| Name | MAI/GENESIS |
| Owner & Operator | GENESIS INDUSTRIES, INC. |
| Contact Address | 303 SOUTH MCKAY AVE., P.O. BOX 39 SPRING VALLEY WI 54767 US |
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 605 Pro-Ject Drive ELMWOOD, WI 54740 US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
| Mai/Genesis | Vaginal Applicator 27586 | 2023-09-22 |
MAI/GENESIS [GENESIS INDUSTRIES, INC.] | EVERT-IT | 2014-11-17 |
MAI/GENESIS [GENESIS INDUSTRIES, INC.] | QUAD-TIP VAGINAL APPLICATOR | 2002-12-09 |
| Import ID | Shipment | Cargo Description | Quantity |
|---|---|---|---|
| 2018060124830 | Hong Kong,Hong Kong -> Seattle, Washington | AURI-KLEEN:SILCONE TUBING ARUI-KLEEN:VACUUM GAUGE AURI-KLEEN:POWER SUPPLY AURI-KLEEN:POWER ORD 31 CTNS (1 PLT) T S CARGO FM KEELUNG TO MINNEAPOLIS VIA HKG | 31 CTN |