Anesthesia Associates, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 2022648
- Devices
- 737
- Registrations
- FDA
- FDA recalls
- 0
What Anesthesia Associates, Inc. makes
Anesthesia Associates, Inc. makes medical devices such as rigid intubation laryngoscopes, low-pressure tubing connectors, breathing circuit connectors, breathing circuit bags, anaesthesia face masks, mechanical expiratory valves, blood pressure cuffs, and oropharyngeal airways. These products include reusable devices like laryngoscopes and breathing circuit bags, as well as single-use items like oropharyngeal airways.
The company's portfolio includes devices classified as Class I and Class II, and its devices are listed in the FDA UDI registry. Anesthesia Associates, Inc. is based in the US.
Catalogue
Search and filter all 737 devicesShowing 1-50 of 737
Company details
- FDA FEI number
- 2022648
- Address
- 460 Enterprise Street, SAN MARCOS, CA, 92078
Frequently asked questions
How many devices does Anesthesia Associates, Inc. have in the registry?
The registry currently lists 737 devices for Anesthesia Associates, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anesthesia Associates, Inc.'s devices?
Among its 50 most recently registered devices, Anesthesia Associates, Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Anesthesia Associates, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Anesthesia Associates, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Anesthesia Associates, Inc. in the registry?
The most recently registered devices listed for Anesthesia Associates, Inc. include AincA® LF-124-50, AincA 00-488, AincA® AP-374-4 and AincA® 00-100-PLUS.