Kappler, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Kappler, Inc. makes
Kappler, Inc. manufactures protective barrier products, including sterile procedure gowns and boot covers designed for use in clinical and procedural environments to reduce contamination risk during medical procedures.
The company’s portfolio is regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. These products are listed in the FDA’s 510(k) database and are intended for use in the United States.
Catalogue
Kappler Pro/Vent Procedure Gown Ref K932694
Regimes: 510(k) Registry: 510(k)Kappler Pro/Vent Boot Ref K932738
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kappler, Inc. have in the registry?
The registry currently lists 2 devices for Kappler, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kappler, Inc.'s devices?
Among its 2 most recently registered devices, Kappler, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Kappler, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kappler, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kappler, Inc. in the registry?
The most recently registered devices listed for Kappler, Inc. include KAPPLER PRO/VENT PROCEDURE GOWN and KAPPLER PRO/VENT BOOT.