Tekna Manufacturing Pvt. Ltd.
FDA Registration(s)#
| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|---|---|---|---|---|---|
| 3013595329 | 3013595329 | Tekna Manufacturing Pvt. Ltd. | 1 | N | 2026-01-01 | C19, Industrial Estate, Guindy Chennai Tamil Nadu IN 600032 |
Registered Device Listings#
| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|---|---|---|---|---|
| 203855 | 2016937451 | K002795 | MODEL HYBRID 3200 MONOPLACE, HYPERBARIC THERAPY SYSTEMS | CBF | 2000-12-06 |
| 203855 | 1194840245 | K002794 | MODEL 5000 MULTIPLACE HYPERBARIC THERAPY | CBF | 2000-12-06 |
| 203855 | 1198164946 |
Product Codes Associated With Registrations#
| Product code | Registration listing records | Latest decision |
|---|---|---|
| CBF | 4 | 2000-12-06 |