FDA device listing
DRE Comfort Series Warmer
FDA device listing 1280461348 · DRE Resume LLC
Key facts
| Proprietary names | DRE Comfort Series Warmer |
|---|---|
| Owner/operator | DRE Resume LLC |
| Owner/operator number | 10092249 |
| Premarket submissions | K080609 |
| Product codes | LHC |
| Device names | LHC - Warmer, Irrigation Solution |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.5950 |
| Review panels | Physical Medicine |
| Registered establishments | DRE Med |
| Establishment registrations | 1000122786 |
| FEI numbers | 1000122786 |
| Establishment operations | Repackager/Relabeler |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 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