Charles Polo & Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Charles Polo & Co., Inc. makes
Charles Polo & Co., Inc. manufactures surgical lighting accessories and insufflation tubing, including both sterile and non-sterile variants. These products support minimally invasive procedures by providing illumination and gas delivery systems.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Light, Surgical Accessories Ref K882132
Regimes: 510(k) Registry: 510(k)Insufflation Tubing Sterile And Non-Sterile Ref K935639
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Charles Polo & Co., Inc. have in the registry?
The registry currently lists 2 devices for Charles Polo & Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Charles Polo & Co., Inc.'s devices?
Among its 2 most recently registered devices, Charles Polo & Co., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Charles Polo & Co., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Charles Polo & Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Charles Polo & Co., Inc. in the registry?
The most recently registered devices listed for Charles Polo & Co., Inc. include LIGHT, SURGICAL ACCESSORIES and INSUFFLATION TUBING STERILE AND NON-STERILE.