Kelleher Corp.
United StatesFDA applicant, unverified
- Devices
- 94
What Kelleher Corp. makes
Kelleher Corp. manufactures specialized surgical instruments and devices for otolaryngology (ENT) and microsurgery, including lancets for ear procedures, adentomes, tonsil dissectors, and microscurgical tools. Their portfolio also covers laryngostroboscopes, myringotomy knives, tracheostomy sets, and related ENT forceps and currettes. Light sources and automated treatment chairs for procedural use are also part of their offerings.
The company’s devices are regulated under FDA’s 510(k) pathway, with products classified as Class I and Class II. Their instruments are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. medical device regulations. The manufacturer operates from the United States.
Catalogue
Search and filter all 94 devicesShowing 1-50 of 94
Frequently asked questions
How many devices does Kelleher Corp. have in the registry?
The registry currently lists 94 devices for Kelleher Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kelleher Corp.'s devices?
Among its 50 most recently registered devices, Kelleher Corp. has devices listed in FDA 510(k) (50 devices).
What risk classes do Kelleher Corp.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Kelleher Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kelleher Corp. in the registry?
The most recently registered devices listed for Kelleher Corp. include NAGASHIMA LIGHT SOURCE UNIT SL-5, LANCETS FOR EAR SURGERY, ADENOTOMES and TONSIL DISSECTORS.