Data / Medical devices / United States / General Aesthetic Manufacturing
General Aesthetic Manufacturing: FDA-registered device maker in Park City, UT, United States, 1 510(k) clearance
General Aesthetic Manufacturing is registered with the FDA (registration 3035375056) in Park City, UT, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 2, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3035375056
- Address
- 4383 N. Forestdale Dr., Park City, UT, United States, 84098
- Owner or operator
- General Aesthetic Manufacturing, LLC (10092443)
- Roles
- Specification developer
- First device listed
- January 8, 2025
- Registered through
- 2026
- Brand names listed
- Sentient Laser Fiber
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 2, 2022 | K213554 | Sentient Manufacturing Laser Fiber | GEX | Substantially Equivalent | Sentient Manufacturing , LLC | accessdata.fda.gov |
Compare with other makers
Updated February 2, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.