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Data / Medical devices / Massager, Therapeutic, Manual / United States

FDA-registered makers of Massager, Therapeutic, Manual in the United States: 29 establishments

29 establishments in the United States are registered with the FDA to make Massager, Therapeutic, Manual (product code LYG). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Massager, Therapeutic, Manual
Product code
LYG
Country
United States

Makers of Massager, Therapeutic, Manual in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
3-Point Products, Inc.Stevensville, MD, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
ARK Products, LLCColumbia, SC, United StatesManufacturer0000api.fda.gov
Ashley Black Inc.Houston, TX, United StatesSpecification developer0000api.fda.gov
Bionix, LLCMaumee, OH, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Capture Accessories, LLCNew York, NY, United StatesSpecification developer0000api.fda.gov
Contour Products IncCharlotte, NC, United StatesSpecification developer0000api.fda.gov
Core Products Intl., Inc.Osceola, WI, United StatesManufacturer0000api.fda.gov
Chirp Innovation, LLCLehi, UT, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Core Products International IncChetek, WI, United StatesManufacturer0000api.fda.gov
Erchonia CorporationFountain Inn, SC, United StatesComplaint file establishment, Manufacturer, Remanufacturer0000api.fda.gov
Fit For Life, LLCEmpire State, NY, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
FridaBaby LLCMiami, FL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Global TV Concepts, Ltd.Coconut Creek, FL, United StatesSpecification developer0000api.fda.gov
Implus Footcare LLCDurham, NC, United StatesSpecification developer0000api.fda.gov
Kmi Imi Group / Dba: Innovative Med, Inc.Irvine, CA, United StatesManufacturer0000api.fda.gov
Medi-Dyne Healthcare Products, Inc.Colleyville, TX, United StatesSpecification developer0000api.fda.gov
Merchsource LLCIrvine, CA, United StatesSpecification developer0000api.fda.gov
Medbio Orchard ParkOrchard Park, NY, United StatesContract manufacturer0000api.fda.gov
Nobol, Inc.Yorba Linda, CA, United StatesContract manufacturer0000api.fda.gov
North Coast Medical, Inc.Morgan Hill, CA, United StatesManufacturer0000api.fda.gov
Revere Plastics Systems, LLCMcPherson, KS, United StatesContract manufacturer0000api.fda.gov
Richardson Products, Inc.Frankfort, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Roll Recovery, LLCBoulder, CO, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Scholl's Wellness CompanyParsippany, NJ, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Smart Tools Plus LlcNorth Royalton, OH, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Talbot's Pharmaceuticals Family Products LLCMonroe, LA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
The Hygenic Company, LLCAkron, OH, United StatesSpecification developer0000api.fda.gov
Thrival LLCSomers, MT, United StatesComplaint file establishment, Specification developer0000api.fda.gov
XF Agencija US Inc.Chicago, IL, United StatesSpecification developer0000api.fda.gov

Updated November 3, 2026. 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.