James L. Geraci & Associates, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What James L. Geraci & Associates, Inc. makes
James L. Geraci & Associates, Inc. supplies medical devices including myringotomy tubes for ear drainage, surgical drapes for sterile field protection, and pneumatic equipment for filtration and smoke evacuation in surgical settings. Their portfolio also covers laser systems for medical procedures and air filtration controls for operating room environments.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company operates within the United States.
Catalogue
Carl Zeiss Inn Myringotomy Tube Line Ref K811698
Regimes: 510(k) Registry: 510(k)Airmed Pneumatic Equip. Filtra/Control Ref K820079
Regimes: 510(k) Registry: 510(k)Drape, Surgical Ref K820078
Regimes: 510(k) Registry: 510(k)Airmed Smoke Evacuation & Filter Ref K820091
Regimes: 510(k) Registry: 510(k)Lase System Ii Ref K853927
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does James L. Geraci & Associates, Inc. have in the registry?
The registry currently lists 5 devices for James L. Geraci & Associates, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list James L. Geraci & Associates, Inc.'s devices?
Among its 5 most recently registered devices, James L. Geraci & Associates, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do James L. Geraci & Associates, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for James L. Geraci & Associates, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from James L. Geraci & Associates, Inc. in the registry?
The most recently registered devices listed for James L. Geraci & Associates, Inc. include CARL ZEISS INN MYRINGOTOMY TUBE LINE, AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL, DRAPE, SURGICAL and AIRMED SMOKE EVACUATION & FILTER.