FDA device listing
Glow
FDA device listing 1794644379 · Upward Labs Holdings Inc.
Key facts
| Proprietary names | Glow |
|---|---|
| Owner/operator | Upward Labs Holdings Inc. |
| Owner/operator number | 10082437 |
| Product codes | LHD |
| Device names | LHD - Device, Fertility Diagnostic, Proceptive |
| Device class | Unclassified |
| Classification regulations (21 CFR) | ORCA1.LHD |
| Review panels | Obstetrics/Gynecology |
| Registered establishments | UPWARD LABS HOLDINGS INC. |
| Establishment registrations | 3020161798 |
| FEI numbers | 3020161798 |
| Establishment operations | Complaint File Establishment |
| 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