Contract manufacturerResMed Corp (Lithia Spgs, GA)GeorgiaAnesthesiologyClass IClass II
ResMed Corp
Contract manufacturer · Lithia Spgs, GA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3011205710 (openFDA record; or search FDA's registration database)
- FEI number
- 3011205710
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- RESMED CORP. (FDA owner/operator no. 9002319)
- Registered address
- 600 Riverside Parkway Suite 100, Lithia Spgs, GA 30122
- Contract listings
- 15 device listings, 7 product codes, first listed Jan 25, 2007
- 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 |
|---|---|---|---|---|---|
| BYX | Tubing, Pressure And Accessories | Class I | Anesthesiology | Contract manufacturing | Jan 25, 2007 |
| BZD | Ventilator, Non-Continuous (Respirator) | Class II | Anesthesiology | Contract manufacturing | Nov 5, 2009 |
| CAW | Generator, Oxygen, Portable | Class II | Anesthesiology | Contract manufacturing | Nov 14, 2016 |
| CBK | Ventilator, Continuous, Facility Use | Class II | Anesthesiology | Contract manufacturing | Jul 18, 2016 |
| MNR | Ventilatory Effort Recorder | Class II | Anesthesiology | Contract manufacturing | May 13, 2014 |
| MNS | Ventilator, Continuous, Non-Life-Supporting | Class II | Anesthesiology | Contract manufacturing | Mar 24, 2013 |
| NOU | Continuous, Ventilator, Home Use | Class II | Anesthesiology | Contract manufacturing | Jul 18, 2016 |