FDA device listing
Podimetrics Remanufactured SmartMat (Model PMHS201U-R),Podimetrics SmartMat (Model PMHS200U),Podimetrics SmartMat (Model…
FDA device listing 1754327725 · Podimetrics, Inc.
Key facts
| Proprietary names | Podimetrics Remanufactured SmartMat (Model PMHS201U-R),Podimetrics SmartMat (Model PMHS200U),Podimetrics SmartMat (Model PMHS201U),Podimetrics SmartMat+ (PMHS300U),Podimetrics Wi-Fi SmartMat (Model PMHS230U) |
|---|---|
| Owner/operator | Podimetrics, Inc. |
| Owner/operator number | 10051975 |
| Product codes | OIZ |
| Device names | OIZ - Foot Examination Tool For Inflammatory Changes |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.5050 |
| Review panels | Physical Medicine |
| Registered establishments | PODIMETRICS, INC. |
| Establishment registrations | 3012492422 |
| FEI numbers | 3012492422 |
| Establishment operations | Complaint File Establishment, Specification Developer |
| 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