Data / Medical devices / United States / Michael Todd Beauty, LP
Michael Todd Beauty, LP: FDA-registered device maker in Port St Lucie, FL, United States, 3 510(k) clearances
Michael Todd Beauty, LP is registered with the FDA (registration 3011547157) in Port St Lucie, FL, United States. It lists 6 device types. The FDA files 3 510(k) clearances under its listings, the newest dated May 31, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011547157
- Address
- 584 NW University Blvd Suite 600, Port St Lucie, FL, United States, 34986
- Owner or operator
- Michael Todd Beauty (10059304)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- December 19, 2018
- Registered through
- 2026
- Brand names listed
- BIOMIST MD, Bella, Claro, Clear Bi-Light, Clear Max Nasal Salt, LEXI IPL (Model: LX-1917), LUMOS IPL, MIO and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blade, Scalpel | GES | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Dermatome | GFD | 1 | Specification developer | accessdata.fda.gov |
| Humidifier, Non-Direct Patient Interface (Home-Use) | KFZ | 1 | Specification developer | accessdata.fda.gov |
| Irrigator, Powered Nasal | KMA | 1 | Specification developer | accessdata.fda.gov |
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Specification developer | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 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 |
|---|---|---|---|---|---|---|
| May 31, 2024 | K240969 | IPL Hair Removal (SL-B287, SL-B329, SL-B301-1, SL-B328) | OHT | Substantially Equivalent | Shenzhen Semlamp Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| July 7, 2022 | K221246 | IPL Hair Removal (Model: SL-B080, SL-B126, SL-B136) | OHT | Substantially Equivalent | Shenzhen Semlamp Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| February 15, 2016 | K153081 | Clear Bi-Light | OLP | Substantially Equivalent | Michael Todd, LP | accessdata.fda.gov |
Compare with other makers
- All makers of Dermatome
- All makers of Over-The-Counter Powered Light Based Laser For Acne
- All makers of Light Based Over-The-Counter Hair Removal
- All makers of Blade, Scalpel
- All makers of Humidifier, Non-Direct Patient Interface (Home-Use)
- All makers of Irrigator, Powered Nasal
Updated May 31, 2024. 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.