# Mackay Manufacturing, Inc. (contract manufacturer, Spokane Valley, WA): 11 new FDA device listings, incl. orthopedic stereotaxic instrument

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Mackay Manufacturing, Inc. |
| Owner / operator | MacKay Manufacturing, Inc. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Spokane Valley, WA, US |
| New listings | 11 |
| Devices | Orthopedic Stereotaxic Instrument; Neurosurgical Nerve Locator; Stimulator, Electrical, Evoked Response; Electrode, Cutaneous; Electromyograph, Diagnostic; Electrode, Needle; Stimulator, Nerve; Intervertebral Fusion Device With Bone Graft, Cervical |
| Product codes | OLO, PDQ, GWF, GXY, IKN, GXZ, ETN, ODP |
| Device classes | Class II |
| Medical specialties | Neurology, Ear, Nose, Throat, Physical Medicine, Orthopedic |
| First new listing | 2026-08-12 |
| Latest new listing | 2026-08-17 |
| FDA registration number | 3003935342 |
| Registration expires | 2027-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.

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: 2026-11-04T21:52:36.524Z.
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.