FDA device listing
Applicator OP 155S,ChiroGold,OW100S, OrthoGold, DermaGold,SoftWave Gold,SoftWave Gold Li
FDA device listing 1873525554 · TISSUE REGENERATION TECHNOLOGIES, LLC
Key facts
| Proprietary names | Applicator OP 155S,ChiroGold,OW100S, OrthoGold, DermaGold,SoftWave Gold,SoftWave Gold Li |
|---|---|
| Owner/operator | TISSUE REGENERATION TECHNOLOGIES, LLC |
| Owner/operator number | 9094965 |
| Premarket submissions | K213120 |
| Product codes | ISA |
| Device names | ISA - Massager, Therapeutic, Electric |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.5660 |
| Review panels | Physical Medicine |
| Registered establishments | SOFTWAVE TISSUE REGENERATON TECHNOLOGIES, LLC |
| Establishment registrations | 3006066512 |
| FEI numbers | 3006066512 |
| Establishment operations | Complaint File Establishment, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 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