Consolidated Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 20
What Consolidated Technologies, Inc. makes
Consolidated Technologies, Inc. manufactures immunoassay controls, urine chemistry controls, and reference materials for drug testing, including sets for AFP, CRP, H. pylori, THC-COOH, and phencyclidine in human urine. Products include lyophilized chemistry controls, serum control sets, and multi-level controls for laboratory quality assurance and validation.
The company’s portfolio is regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. Products are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Search and filter all 20 devicesFrequently asked questions
How many devices does Consolidated Technologies, Inc. have in the registry?
The registry currently lists 20 devices for Consolidated Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Consolidated Technologies, Inc.'s devices?
Among its 20 most recently registered devices, Consolidated Technologies, Inc. has devices listed in FDA 510(k) (20 devices).
What risk classes do Consolidated Technologies, Inc.'s devices fall under?
Among its 20 most recently registered devices, the classes recorded for Consolidated Technologies, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Consolidated Technologies, Inc. in the registry?
The most recently registered devices listed for Consolidated Technologies, Inc. include QUALITROL DHP IMMUNOASSAY CONTROL LEVELS 1, 2 AND 3, CONFORMANCEE MCC-LIGAND CONTROL LEVELS 1, 2 AND 3, QUALITROL, (ALFA FETOPROTEIN) AFP CONTROL SET, QUALITROL RF CONTROLS and QUALITROL SYPHSERO CONTROL SET.