FDA device listing
4 WAY STRETCH ELBOW SUPPORT BLACK L/XL,4 WAY STRETCH ELBOW SUPPORT BLACK S/M,ADJUSTABLE ELBOW SUPPORT,ADJUSTABLE ELBOW…
FDA device listing 1098551237 · MUELLER SPORTS MEDICINE, INC.
Key facts
| Proprietary names | 4 WAY STRETCH ELBOW SUPPORT BLACK L/XL,4 WAY STRETCH ELBOW SUPPORT BLACK S/M,ADJUSTABLE ELBOW SUPPORT,ADJUSTABLE ELBOW SUPPORT GREEN LINE OSFM,ADJUST-TO-FIT TENNIS ELBOW SUPPORT OSFM,DIAMOND PAD ELBOW SLEEVE BK REG,DIAMOND PAD ELBOW SLEEVE WHT SM,ELASTIC ELBOW SUPPORT BLACK LARGE,ELASTIC ELBOW SUPPORT BLACK MEDIUM,ELASTIC ELBOW SUPPORT BLACK SMALL,ELASTIC ELBOW SUPPORT BLACK X-LARGE,ELBOW SLEEVE… |
|---|---|
| Owner/operator | MUELLER SPORTS MEDICINE, INC. |
| Owner/operator number | 2110420 |
| Product codes | IOY |
| Device names | IOY - Support, Arm |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3475 |
| Review panels | Physical Medicine |
| Registered establishments | MUELLER SPORTS MEDICINE, INC. |
| Establishment registrations | 2110420 |
| FEI numbers | 2110420 |
| Establishment operations | Complaint File Establishment, Manufacturer, Repackager/Relabeler, 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