Contract manufacturerSTERIS CORPORATION (Mentor, OH)OhioGeneral hospitalClass II
STERIS CORPORATION
Contract manufacturer ยท Mentor, OH
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3004080920 (openFDA record; or search FDA's registration database)
- FEI number
- 3004080920
- Registered for
- FDA registration year 2026
- Establishment types
- Complaint file establishment; Specification developer; Manufacturer for export only; Manufacturer; Contract manufacturer; Repackager or relabeler
- Owner or operator
- STERIS Corporation (FDA owner/operator no. 10078069)
- Registered address
- 9325 Pinecone Drive, Mentor, OH 44060
- Contract listings
- 2 device listings, 1 product codes, first listed Jun 21, 2023
- 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 |
|---|---|---|---|---|---|
| FRC | Indicator, Biological Sterilization Process | Class II | General hospital | Contract manufacturing | Jun 21, 2023 |