Establishment registration
PRYTIME MEDICAL DEVICES, INC.
FDA establishment registration 3012279212 · Lakewood, US
Key facts
| Registration number | 3012279212 |
|---|---|
| Establishment name | PRYTIME MEDICAL DEVICES, INC. |
| Owner/operator | Prytime Medical Devices, Inc. |
| Owner/operator number | 10050783 |
| FEI number | 3012279212 |
| Address | 575 Union Blvd Suite 107 |
| City | Lakewood |
| State | CO |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | DQO, DQY, MJN, OFC |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- 1–9 FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database