FDA device listing
APEXPULSE,Disposable Pulse Irrigation Kits,PULSAR II,Pulsar II AWI,Pulsar II-S,Pulse Lavage Fan - Spray Kit,SmartPulse
FDA device listing 1760909195 · Apex (Guangzhou) Tools & Orthopedics Company
Key facts
| Proprietary names | APEXPULSE,Disposable Pulse Irrigation Kits,PULSAR II,Pulsar II AWI,Pulsar II-S,Pulse Lavage Fan - Spray Kit,SmartPulse |
|---|---|
| Owner/operator | Apex (Guangzhou) Tools & Orthopedics Company |
| Owner/operator number | 10026676 |
| Product codes | FQH |
| Device names | FQH - Lavage, Jet |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.5475 |
| Review panels | General Hospital |
| Registered establishments | Apex (Guangzhou) Tools & Orthopedics Company |
| Establishment registrations | 3007125392 |
| FEI numbers | 3007125392 |
| Establishment operations | Contract Manufacturer, 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