FDA device listing
ORAcollect Dx (OCD-100, OCD-100A)
FDA device listing 1680089497 · ORASURE TECHNOLOGIES, INC.
Key facts
| Proprietary names | ORAcollect Dx (OCD-100, OCD-100A) |
|---|---|
| Owner/operator | ORASURE TECHNOLOGIES, INC. |
| Owner/operator number | 9000083 |
| Premarket submissions | K152464 |
| Product codes | OYJ |
| Device names | OYJ - Dna Specimen Collection, Saliva |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1675 |
| Review panels | Clinical Chemistry |
| Registered establishments | ORASURE TECHNOLOGIES INC., ORASURE TECHNOLOGIES, INC. |
| Establishment registrations | 3004142665, 3022474803 |
| FEI numbers | 3004142665, 3022474803 |
| Establishment operations | Contract Manufacturer, Repackager/Relabeler |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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