Lca, Inc.
United StatesFDA applicant, unverified
- Devices
- 12
What Lca, Inc. makes
Lca, Inc. manufactures surgical laser systems and accessories, including closed-end fiberoptic laser delivery devices, contact laser systems for ophthalmic procedures, and electrosurgical tools like a padless pencil and modified alloy scalpel handpieces. Their portfolio also covers hybrid surgical devices, laser forceps handpieces, and smoke evacuation suction wands for surgical smoke management.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Their products are based in the United States and appear in the FDA’s 510(k) registry.
Catalogue
Search and filter all 12 devicesFrequently asked questions
How many devices does Lca, Inc. have in the registry?
The registry currently lists 12 devices for Lca, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lca, Inc.'s devices?
Among its 12 most recently registered devices, Lca, Inc. has devices listed in FDA 510(k) (12 devices).
What risk classes do Lca, Inc.'s devices fall under?
Among its 12 most recently registered devices, the classes recorded for Lca, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lca, Inc. in the registry?
The most recently registered devices listed for Lca, Inc. include HYBRID SURGICAL DEVICE MODIFICATION, CLOSED END FIBEROPTIC LASER DELIVERY SYSTEM, CL-OPE CONTACT LASER SYSTEM and LASER FORCEPS HANDPIECE.