FDA device listing
Full Semen Analysis + Cryopreservation Kit,Full Semen Analysis Kit,Vasectomy Kit
FDA device listing 2043263105 · Fellow Health Inc.
Key facts
| Proprietary names | Full Semen Analysis + Cryopreservation Kit,Full Semen Analysis Kit,Vasectomy Kit |
|---|---|
| Owner/operator | Fellow Health Inc. |
| Owner/operator number | 10085317 |
| Product codes | KDT |
| Device names | KDT - Container, Specimen Mailer And Storage, Sterile |
| Device class | Class I |
| Classification regulations (21 CFR) | 864.3250 |
| Review panels | Pathology |
| Registered establishments | FELLOW HEALTH INC. |
| Establishment registrations | 3022897868 |
| FEI numbers | 3017876253 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database