FDA device listing
Thermal Angel
FDA device listing 1098074535 · ESTILL MEDICAL TECHNOLOGIES, INC.
Key facts
| Proprietary names | Thermal Angel |
|---|---|
| Owner/operator | ESTILL MEDICAL TECHNOLOGIES, INC. |
| Owner/operator number | 9036068 |
| Premarket submissions | K012031 |
| Product codes | BSB, LGZ |
| Device names | BSB - Warmer, Blood, Non-Electromagnetic Radiation, LGZ - Warmer, Thermal, Infusion Fluid |
| Device class | Class II |
| Classification regulations (21 CFR) | 864.9205, 880.5725 |
| Review panels | General Hospital, Hematology |
| Registered establishments | ESTILL MEDICAL TECHNOLOGIES, INC. |
| Establishment registrations | 1650754 |
| FEI numbers | 3002587972 |
| Establishment operations | Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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