Longport, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Longport, Inc. makes
Longport, Inc. manufactures the Longport Episcan (Model I-200), a diagnostic imaging device used for endoscopic procedures, and the Longport Model LDS-1, a laser-based surgical device for tissue ablation or coagulation.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Longport Episcan, Model-I-200 Ref K062571
Regimes: 510(k) Registry: 510(k)Longport Model Lds -1 Ref K990238
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Longport, Inc. have in the registry?
The registry currently lists 2 devices for Longport, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Longport, Inc.'s devices?
Among its 2 most recently registered devices, Longport, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Longport, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Longport, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Longport, Inc. in the registry?
The most recently registered devices listed for Longport, Inc. include LONGPORT EPISCAN, MODEL-I-200 and LONGPORT MODEL LDS -1.