FDA device listing
88 Coreset_C111 and HT111,Dr.Coreset_P88,Dr.Coreset Pro_R1090,Miss Poly_BB484,Mr.Poly_SM880
FDA device listing 1847609980 · Slimminggo Group
Key facts
| Proprietary names | 88 Coreset_C111 and HT111,Dr.Coreset_P88,Dr.Coreset Pro_R1090,Miss Poly_BB484,Mr.Poly_SM880 |
|---|---|
| Owner/operator | Slimminggo Group |
| Owner/operator number | 10047363 |
| Product codes | ILH |
| Device names | ILH - Splint, Hand, And Components |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.3475 |
| Review panels | Physical Medicine |
| Registered establishments | Slimminggo Group |
| Establishment registrations | 3011189230 |
| FEI numbers | 3011189230 |
| Establishment operations | Repackager/Relabeler |
| 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