FDA device listing
Dose Cup
FDA device listing 1216051581 · Sturgis Molded Products Company
Key facts
| Proprietary names | Dose Cup |
|---|---|
| Owner/operator | Sturgis Molded Products Company |
| Owner/operator number | 10053177 |
| Product codes | KYX |
| Device names | KYX - Dispenser, Liquid Medication |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.6430 |
| Review panels | General Hospital |
| Registered establishments | STURGIS MOLDED PRODUCTS COMPANY |
| Establishment registrations | 3000170790 |
| FEI numbers | 3000170790 |
| Establishment operations | Contract 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