Xpan, Inc.
CanadaFDA applicant, unverified
Xpan, Inc. is a medical device manufacturer, with 4 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.
- Devices
- 4
Registry facts
- Registries
- FDA GUDID 3
- FDA 510(k) 1
- Device classes
- FDA Class II 4
- Identifiers
- DUNS 208914737
What Xpan, Inc. makes
Xpan, Inc. manufactures single-use laparoscopic access devices, including trocar blades and cannulas designed for minimally invasive surgical procedures. Their products are intended for creating portals in the abdominal wall to facilitate instrument insertion during laparoscopic surgery.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and UDI databases.
Catalogue
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
Xpan Universal Trocar System Ref K223562
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 208914737
Frequently asked questions
How many devices does Xpan, Inc. have in the registry?
The registry currently lists 4 devices for Xpan, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Xpan, Inc.'s devices?
Among its 4 most recently registered devices, Xpan, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Xpan, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Xpan, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Xpan, Inc. in the registry?
The most recently registered devices listed for Xpan, Inc. include Xpan Universal Trocar System XP1076-01, Xpan Universal Trocar System XP1077-01, Xpan Universal Trocar System XP1075-01 and Xpan Universal Trocar System.