Contract manufacturerMyrava, LLC (Parma, OH)OhioRadiologyClass II
Myrava, LLC
Contract manufacturer ยท Parma, OH
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3022973841 (openFDA record; or search FDA's registration database)
- FEI number
- 3022973841
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer
- Owner or operator
- Myrava, Inc. (FDA owner/operator no. 10083421)
- Registered address
- 5575 Venture Drive Unit A, Parma, OH 44130
- Contract listings
- 2 device listings, 2 product codes, first listed Dec 12, 2025
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|
| IYE | Accelerator, Linear, Medical | Class II | Radiology | Contract manufacturing | Dec 12, 2025 |
| QIH | Automated Radiological Image Processing Software | Class II | Radiology | Contract manufacturing | Dec 12, 2025 |