Gibeck, Inc.
United StatesFDA applicant, unverified
- Devices
- 15
What Gibeck, Inc. makes
Gibeck, Inc. manufactures respiratory and ventilatory support devices, including humidification systems (HUMID-VENT series), heated thermal regulation blankets, and related accessories like angled/straight filters, nasal cannula gas sampling devices, and HEPA-filtered heat and moisture exchangers (HMEs). The portfolio also covers disposable CO₂ absorbers and specialized tracheal ventilation components.
The company’s devices are regulated under FDA’s Class I and Class II classifications, with most products cleared via the 510(k) pathway. These products are listed in the FDA’s 510(k) database. Gibeck, Inc. is based in the United States.
Catalogue
Search and filter all 15 devicesFrequently asked questions
How many devices does Gibeck, Inc. have in the registry?
The registry currently lists 15 devices for Gibeck, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gibeck, Inc.'s devices?
Among its 15 most recently registered devices, Gibeck, Inc. has devices listed in FDA 510(k) (15 devices).
What risk classes do Gibeck, Inc.'s devices fall under?
Among its 15 most recently registered devices, the classes recorded for Gibeck, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gibeck, Inc. in the registry?
The most recently registered devices listed for Gibeck, Inc. include HUMID-VENT 1, THERMAL REGULATION SYSTEM BLANKET, HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHT and HUMID-VENT 2.