# Providence Medical Technology, Inc. (manufacturer, Pleasanton, CA): 2 new FDA device listings, incl. orthopedic stereotaxic instrument

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Providence Medical Technology, Inc. |
| Role | Manufacturer |
| Establishment types | Develop Specifications But Do Not Manufacture At This Facility; Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device |
| Location | Pleasanton, CA, US |
| New listings | 2 |
| Devices | Orthopedic Stereotaxic Instrument; System, Facet Screw Spinal Device |
| Product codes | OLO, MRW |
| Device classes | Class II, Unclassified |
| Medical specialties | Neurology |
| Brand names | CORUS Navigation Access System-G2LX; CORUS PCSS 3D Level One; CORUS PCSS 3D Implant |
| First new listing | 2026-05-15 |
| Latest new listing | 2026-10-05 |
| FDA registration number | 3009394448 |
| Registration expires | 2027-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.
- Listed in the last 45 days.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.