Device details
FDA 510(k) registration fields
- K number
- K213554
- Device name
- Sentient Manufacturing Laser Fiber
- Company
- Sentient Manufacturing , LLC
- Country / region
- United States(US)
- Product code
- GEX
- Device class
- Class 2
- Regulation number
- 21 CFR 878.4810
- Date received
- 2021-11-08
- Decision date
- 2022-02-02
- Submission type
- Traditional
- Technology type
- Other(AI inferred)
- Clinical applications
- Surgical cutting
- Primary application
- Surgical cutting
- Classification source
- AI classified