Reprolife America, LLC
FDA Registration(s)#
| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|---|---|---|---|---|---|
| 3018010054 | 3018010054 | Reprolife America, LLC | 1 | N | 2026-01-01 | 22751 Professional Dr Ste 220 Kingwood TX US 77339 |
Registered Device Listings#
| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|---|---|---|---|---|
| 334450 | 1372776948 | K233846 | Vitrification Solution Set and Warming Solution Set | MQL | 2024-08-27 |
Product Codes Associated With Registrations#
| Product code | Registration listing records | Latest decision |
|---|---|---|
| MQL | 1 | 2024-08-27 |