FDA device listing
EVO microneedle
FDA device listing 1500966303 · Shenzhen king medical packaging sterilization service Co.ltd
Key facts
| Proprietary names | EVO microneedle |
|---|---|
| Owner/operator | Shenzhen king medical packaging sterilization service Co.ltd |
| Owner/operator number | 10053058 |
| Product codes | QAI |
| Device names | QAI - Powered Microneedle Device |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4430 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Dongguan King Medical Technology Co.,Ltd |
| Establishment registrations | 3017896194 |
| FEI numbers | 3017896194 |
| Establishment operations | Contract Sterilizer |
| 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