Sharplan Industries, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Sharplan Industries, Inc. makes
Sharplan Industries, Inc. manufactures Nd:YAG surgical lasers designed for precision tissue ablation in gastrointestinal, urological, neurosurgical, and pulmonary procedures. These devices are intended for controlled laser energy delivery in minimally invasive surgeries.
The company’s portfolio consists of Class II medical devices, authorised via the FDA’s 510(k) pathway. These lasers are listed under the relevant regulatory registries for surgical lasers in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sharplan Industries, Inc. have in the registry?
The registry currently lists 4 devices for Sharplan Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sharplan Industries, Inc.'s devices?
Among its 4 most recently registered devices, Sharplan Industries, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Sharplan Industries, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Sharplan Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sharplan Industries, Inc. in the registry?
The most recently registered devices listed for Sharplan Industries, Inc. include MODEL 2100 ND:YAG SURGICAL LASER GASTROINTESTINAL, MODEL 2100 ND:YAG SURGICAL LASER UROLOGICAL INDICA, MODEL 2100 ND:YAG SURGICAL LASER NEUROSURGICAL IND and MODEL 2100 ND:YAG SURGICAL LASER PULMONARY INDICAT.