FDA device listing

BTE Hearing Aid (model: J-307B, J-308B, J-309B, J-310B, J-311B, J-312B, J-313B, J-315B, J-316B, J-317B, J-318B…

FDA device listing 1697765002 · Guangdong Jiajianle Technology Co., Ltd.

Key facts

Proprietary names BTE Hearing Aid (model: J-307B, J-308B, J-309B, J-310B, J-311B, J-312B, J-313B, J-315B, J-316B, J-317B, J-318B, J-319B),BTE Hearing Aid (model: J-320B, J-321B, J-322B, J-323B, J-325B, J-326B),BTE Hearing Aid (model: J-883DB, J-885DB, J-886DB, J-887DB, J-888DB, J-889DB, J-301B, J-302B, J-303B, J-305B, J-306B),BTE Hearing Aid (model: J-961DB, J-962DB, J-963DB, J-965DB, J-966DB, J-967DB, J-968DB…
Owner/operator Guangdong Jiajianle Technology Co., Ltd.
Owner/operator number 10089836
Product codes QUG
Device names QUG - Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter
Device class Class II
Classification regulations (21 CFR) 874.3305
Review panels Ear, Nose, & Throat
Registered establishments GUANGDONG JIAJIANLE TECHNOLOGY CO., LTD.
Establishment registrations 3030535004
FEI numbers 3030535004
Establishment operations Foreign Exporter, Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed 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

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