Bentley Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 58
What Bentley Laboratories, Inc. makes
Bentley Laboratories, Inc. manufactures medical devices including oxygen saturation meters, cardiotomy reservoirs, venous reservoir bags, and arterial blood filters for pediatric and adult use. Their portfolio also covers bubble oxygenation systems for infants, physiological pressure transducers, continuous blood processors, and anesthesia-related equipment. Additional products include flush flow devices and pulse generators for medical monitoring.
The company’s devices are classified under FDA categories Class I, Class II, and Class III, with regulatory submissions recorded in the FDA’s 510(k) clearance database. These products are intended for use in critical care, surgical, and anesthesia settings, adhering to U.S. medical device regulations. The manufacturer is based in the United States.
Catalogue
Search and filter all 58 devicesShowing 1-50 of 58
Frequently asked questions
How many devices does Bentley Laboratories, Inc. have in the registry?
The registry currently lists 58 devices for Bentley Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bentley Laboratories, Inc.'s devices?
Among its 50 most recently registered devices, Bentley Laboratories, Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do Bentley Laboratories, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Bentley Laboratories, Inc.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Bentley Laboratories, Inc. in the registry?
The most recently registered devices listed for Bentley Laboratories, Inc. include OXYGEN SATURATION METER MODEL NO. SM-1, UNIVOX W/HOLDERS, MODELS UNIVOX-HL, HLB, HLF, Q220F CARDITOMY RESERVOIR/MODIFIED and FLUSHFLO II.