FDA Device Establishments · JSON-LD · Markdown

AQP ONE, INC.

FEI 3017415521 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active

FEI Number3017415521
Owner / OperatorAQP ONE, INC. (#10090383)
Address11555 MONARCH STREET, Garden Grove, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)ISA
Regulation § (21 CFR)890.5660
Proprietary namesJBA-VRW LLLT Watch for Vessel Restore – No Pad; JBA-BELT Red and Infrared Light Pain Relief Belt; JBA-PBH LLLT Pain Relief Handheld Device; JBA-FEET LLLT Red and Infrared Light Pain Relief Device for Feet; JBA-SBH LLLT LED Skin Handheld Device; JBA-HEAD LLLT Red and Infrared Light Cap; JBA-VPW LLLT Watch for Vessel Restore and Pain Relief with Pads; JBA-VH LED Gynecological Therapy Device for Vaginal Health; JBA-ACU LLLT Pain Relief Device

External sources

Source: openFDA. Public-domain (CC0).