FDA device listing
PDI Adhesive Tape Remover Pad
FDA device listing 1937858236 · Professional Disposables International, Inc.
Key facts
| Proprietary names | PDI Adhesive Tape Remover Pad |
|---|---|
| Owner/operator | Professional Disposables International, Inc. |
| Owner/operator number | 2411192 |
| Product codes | KOX |
| Device names | KOX - Solvent, Adhesive Tape |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4730 |
| Review panels | General & Plastic Surgery |
| Registered establishments | PROFESSIONAL DISPOSABLES INTERNATIONAL, INC. |
| Establishment registrations | 2411192, 3015361761 |
| FEI numbers | 2411192, 3015361761 |
| 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