Patton Surgical Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Patton Surgical Corp. makes
Patton Surgical Corp. manufactures surgical trocars and related laparoscopic accessories, including the POLARCOAT coating system and various trocar designs such as the PASPORT Optical Trocar, Vortex Seal, Blunt Tip Trocar, Shielded Trocar, and Cannula Anchor. These devices are intended for use in minimally invasive procedures to facilitate instrument insertion and seal gas retention within the abdominal cavity.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. The portfolio is listed in the FDA’s 510(k) database, reflecting compliance with U.S. regulatory requirements. The manufacturer is based in the United States.
Catalogue
Polarcoat Ref K052907
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Patton Surgical Corp. have in the registry?
The registry currently lists 2 devices for Patton Surgical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Patton Surgical Corp.'s devices?
Among its 2 most recently registered devices, Patton Surgical Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Patton Surgical Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Patton Surgical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Patton Surgical Corp. in the registry?
The most recently registered devices listed for Patton Surgical Corp. include POLARCOAT and PASPORT OPTICAL TROCAR, VORTEX SEAL, BLUNT TIP TROCAR, SHIELDED TROCAR, CANNULA ANCHOR.