FDA device listing
Suture removal kit
FDA device listing 1275542614 · New Pentastar Medical Products Co. Limited
Key facts
| Proprietary names | Suture removal kit |
|---|---|
| Owner/operator | New Pentastar Medical Products Co. Limited |
| Owner/operator number | 10063374 |
| Product codes | MCZ |
| Device names | MCZ - Suture Removal Kit |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | JIANGSU NEW PENTASTAR MEDICAL PRODUCTS CO. LTD. |
| Establishment registrations | 3015058854 |
| FEI numbers | 3015058854 |
| Establishment operations | Foreign Exporter |
| 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