Data / Medical devices / United States / PJM Worldwide, LLC
PJM Worldwide, LLC: FDA-registered device maker in Miami, FL, United States, 3 510(k) clearances
PJM Worldwide, LLC is registered with the FDA (registration 3008855505) in Miami, FL, United States. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated May 22, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008855505
- Address
- 1499 NW 79th Avenue, Miami, FL, United States, 33126
- Owner or operator
- PJM World Wide, LLC DBA Phoenix Medical Technology, LLC (10059366)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- December 27, 2018
- Registered through
- 2026
- Brand names listed
- Booster, Bosley Revitalizer
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Laser, Comb, Hair | OAP | 2 | Repackager or relabeler, 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 22, 2024 | K240456 | Bosley Booster 128 Laser Cap; Bosley Booster 162 Laser Cap; Bosley Booster 288 Laser Cap | OAP | Substantially Equivalent | Plm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC | accessdata.fda.gov |
| January 29, 2020 | K192585 | Bosley Revitalizer 96 Laser Cap, Bosley Revitalizer 96 XL Laser Cap | OAP | Substantially Equivalent | Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC | accessdata.fda.gov |
| August 10, 2018 | K181253 | Bosley Revitalizer 272 Laser Cap, Bosley Revitalizer 164 Laser Cup | OAP | Substantially Equivalent | Pjm Worldwide, LLC D/B/A Phoenix Medical Technology, LLC | accessdata.fda.gov |
Compare with other makers
Updated May 22, 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.