Genie Medical

Sales Pack, Genie Medical Bahs 2024.2 USB

Registry build 21.09.26
4manufacturers in China registered for this device type
3catalogue numbers in this listing
8510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (2), Henan (1), Shanghai (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code LXB
Manufacturer City Province Registered as Device types
Mehow Innovative (Huizhou) Ltd. Huizhou Guangdong Contract manufacturer 11
Zdeer Technology (Henan) Co., Ltd. Xuchang Henan Remanufacturer 9
Shenzen Magnet Technology Co., Ltd. Shenzen Guangdong Manufacturer 2
Sonitus Medical (Shanghai) Co., Ltd. Shanghai Shanghai Specification developer 1

Record

Regulatory record for Genie Medical
Listed by Oticon Medical AB, Sweden
FDA product code LXB
Device type Hearing Aid, Bone Conduction
Device class Class 2
Regulation 21 CFR 874.3302
Establishment Specification developer, Repacker / relabeller, Private-label distributor, Complaint-file establishment, Manufacturer
Record published 2024-08-08

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Genie Medical
Catalogue number Size Status
275203 In distribution
275351 In distribution
275209 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Ponto Oticon Medical AB 172
Hearing Aid, Bone Conduction BHM-Tech Produktionsgesellschaft m.b.H. 99
Baha Cochlear Bone Anchored Solutions AB 98
Otomag™ Attract™ Magnetic Spacer Medtronic Xomed, Inc. 23
Attract™ Medtronic Xomed, Inc. 22
Otomag™ Alpha 2 Sound Processor Medtronic Xomed, Inc. 21
Hearing Aid, Bone Conduction Medtronic Xomed, Inc. 21
contact BHM-Tech Produktionsgesellschaft m.b.H. 21
contact mini BHM-Tech Produktionsgesellschaft m.b.H. 12
Otomag™ Alpha (M) Magnetic Implant Medtronic Xomed, Inc. 6
contact forte Alpha BHM-Tech Produktionsgesellschaft m.b.H. 5
contact forte BHM-Tech Produktionsgesellschaft m.b.H. 5

Showing 12 of 230. All products under Hearing Aid, Bone Conduction

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K213733 2021-12-16
K211640 2021-08-10
K190540 2019-05-02
K161671 2016-09-29
K132775 2013-12-09
K103594 2011-06-15
K090996 2009-07-29
K082108 2008-11-14

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer