LightScalpel
Powered Laser Surgical Instrument
LightScalpel LLC
The following data is part of a premarket notification filed by Lightscalpel Llc with the FDA for Lightscalpel.
Pre-market Notification Details
| Device ID | K173827 |
| 510k Number | K173827 |
| Device Name: | LightScalpel |
| Classification | Powered Laser Surgical Instrument |
| Applicant | LightScalpel LLC 11818 North Creek Parkway N Suite 100 Bothell, WA 98011 |
| Contact | David Walters |
| Correspondent | David Walters LightScalpel LLC 11818 North Creek Parkway N Suite 100 Bothell, WA 98011 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-12-18 |
| Decision Date | 2018-09-14 |
| Summary: | summary |
Trademark Results [LightScalpel]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LIGHTSCALPEL 90237948 not registered Live/Pending |
LightScalpel, LLC 2020-10-06 |
 LIGHTSCALPEL 85005837 3889495 Live/Registered |
LightScalpel LLC 2010-04-04 |
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