FDA device listing

Bosley Revitalizer

FDA device listing 1097733368 · PJM World Wide, LLC DBA Phoenix Medical Technology, LLC

Key facts

Proprietary names Bosley Revitalizer
Owner/operator PJM World Wide, LLC DBA Phoenix Medical Technology, LLC
Owner/operator number 10059366
Premarket submissions K181253
Product codes OAP
Device names OAP - Laser, Comb, Hair
Device class Class II
Classification regulations (21 CFR) 890.5500
Review panels Physical Medicine
Registered establishments PJM WORLDWIDE, LLC
Establishment registrations 3008855505
FEI numbers 3008855505
Establishment operations Specification Developer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

Browse all FDA device listings