FDA device listing
Circumcision Stapler for Single Use
FDA device listing 1223348565 · PREMIUM PLUS DENTAL
Key facts
| Proprietary names | Circumcision Stapler for Single Use |
|---|---|
| Owner/operator | PREMIUM PLUS DENTAL |
| Owner/operator number | 10027069 |
| Product codes | FLG, GDT |
| Device names | FLG - Cleaner, Ultrasonic, Medical Instrument, GDT - Staple, Removable (Skin) |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4760, 880.6150 |
| Review panels | General Hospital, General & Plastic Surgery |
| Registered establishments | PREMIUM PLUS DENTAL SUPPLIES INC, TOUCHSTONE INTERNATIONAL MEDICAL SCIENCE CO., LTD. |
| Establishment registrations | 3004425647, 3007222388 |
| FEI numbers | 3004425647, 3007222388 |
| Establishment operations | Complaint File Establishment, Manufacturer |
| 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