# Resmed Corp (manufacturer, San Diego, CA): 9 new FDA device listings, incl. accessory to continuous ventilator (respirator)

**Score:** 95/100

| Field | Value |
|---|---|
| Establishment | Resmed Corp |
| Owner / operator | Resmed Corp. |
| Role | Manufacturer |
| Establishment types | Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device |
| Location | San Diego, CA, US |
| New listings | 9 |
| Devices | Accessory To Continuous Ventilator (Respirator); Ventilator, Continuous, Non-Life-Supporting; Ventilator, Non-Continuous (Respirator); Ventilatory Effort Recorder |
| Product codes | MOD, MNS, BZD, MNR |
| Device classes | Class II |
| Medical specialties | Anesthesiology |
| First new listing | 2026-08-10 |
| Latest new listing | 2026-09-30 |
| FDA registration number | 3007573469 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- 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.