Atlas FDA

XOMED AUDIANT BONE CONDUCTOR AT THE EAR SOUND PRO.

FDA 510(k) clearance K872168 · decided 1987-06-30

Clearance details

K-number
K872168
Device name
XOMED AUDIANT BONE CONDUCTOR AT THE EAR SOUND PRO.
Applicant
Xomed, Inc.
Decision
Substantially Equivalent
Date received
1987-06-08
Decision date
1987-06-30
Days to decision
22 days
Clearance type
Traditional
Product code
LXB
Device class
2
Regulation number
874.3302
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Jacksonville, FL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Ossiclear (Ossiclear System) (K254296)Sounduct2026-07-22
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Bone Conduction Hearing Aid (XTS-AISW-D1, XTS-AISW-D2, XTS-AISW-D3) (K261256)Shenzhen Magnet Technology Co., Ltd.2026-06-11
Baha 7 Sound Processor; Baha Fitting Software 7 (P2121898); Baha Smart App (iOS) (P1646054); Baha Smart App (Android) (P1646035); Baha SoundBand (K250215)Cochlear2025-05-29
contact forte Alpha (K243041)Bhm-Tech Produktionsgesellschaft Mbh2025-04-25
Ponto 5 SuperPower (K213733)Oticon Medical AB2021-12-16
Cochlear Baha 6 System, Cochlear Baha Fitting Software 6, Cochlear Baha Baha Smart App (K212136)Cochlear Americas2021-09-29
Ponto 5 Mini (K211640)Oticon Medical AB2021-08-10
Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha Smart App (K202048)Cochlear Americas2021-02-23
Ponto 4 (K190540)Oticon Medical AB2019-05-02
ADHEAR System (K172460)Med-El Elektromedizinische Geraete GmbH2018-04-27
Cochlear Baha SoundArc (K171088)Cochlear Americas2017-06-07

Recalls involving this device

No recalls on record reference this clearance.