Pollux Endoscopy, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Pollux Endoscopy, Inc. makes
Pollux Endoscopy, Inc. manufactures rigid endoscopes for sinus, laparoscopic, and cystoscopic procedures, including the SINUSCOPE with accessories, a laparoscope, and cystoscopes in 0°, 15°, 30°, and 70° angles. The company also produces the POLLUX OA and POLLUX 30A/70A series for orthopedic and arthroscopic applications.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Sinuscope And Baccessories Ref K002214
Regimes: 510(k) Registry: 510(k)Laparascope Ref K943662
Regimes: 510(k) Registry: 510(k)Cystoscope 0/15/30/70 Degrees Ref K960872
Regimes: 510(k) Registry: 510(k)Pollux Oa/Pollux 30A/Pollux 70A Ref K953484
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pollux Endoscopy, Inc. have in the registry?
The registry currently lists 4 devices for Pollux Endoscopy, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pollux Endoscopy, Inc.'s devices?
Among its 4 most recently registered devices, Pollux Endoscopy, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Pollux Endoscopy, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Pollux Endoscopy, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pollux Endoscopy, Inc. in the registry?
The most recently registered devices listed for Pollux Endoscopy, Inc. include SINUSCOPE AND BACCESSORIES, LAPARASCOPE, CYSTOSCOPE 0/15/30/70 DEGREES and POLLUX OA/POLLUX 30A/POLLUX 70A.