510(k) Report

510(k) · Cleared

Cleared

Baha 5 Power Sound Processor

K161123510(k) SpecialCleared May 20, 201629-day reviewClass II21 CFR 874.3302

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Cochlear Americas · LXB Hearing Aid, Bone Conduction

Cleared on May 20, 2016 as substantially equivalent to K110996 (Cochlear Americas, 2011) and 1 other predicate after a 29-day review. Its family tree reaches back 8 generations to 1986. 6 later devices descend from it.

Decided
May 20, 2016
Review
29 days
Class
Class II
Product code
LXB
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K861971 (1986). 20 ancestors in all. 6 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2011: 1 other ancestor2008: 1 other ancestor2004: 1 other ancestor2002: 1 other ancestor2001: 1 other ancestor1999: 1 other ancestor1998: 1 other ancestor1994: 1 other ancestor1993: 1 other ancestor1995: 1 other ancestor1991: 1 other ancestor1987: 1 other ancestor2017: 1 descendant cleared2021: 2 descendants cleared2026: 2 descendants cleared2025: 1 descendant clearedK861971 · Xomed Audiant Bone Conductor W/Improved AA Coil · Xomed, Inc. · 1986K955713 · Nobelpharma Bone Anchored Hearing Aid · Nobelpharma USA, Inc. · 1996×2: 2 generations cleared close together, K984162 (1999), K992872 (1999) K080363 · Baha Cordelle II · Cochlear Bone Anchored Systems AB · 2008K090720 · Cochlear Baha BP100 · Cochlear Bone Anchored Systems AB · 2009K132278 · Cochlear Baha 4 Sound Processor · Cochlear Americas · 2013K142907 · Baha 5 Sound Processor · Cochlear Americas · 2015 · recalled1990200020102020
  1. Root · 8 generations backK861971 Xomed Audiant Bone Conductor W/Improved AA CoilXomed, Inc. · 1986
  2. 7 generations backK955713 Nobelpharma Bone Anchored Hearing AidNobelpharma USA, Inc. · 1996
  3. 6 generations backK984162 Branemark Bone-Anchored Hearing Aid (Baha) System for Pediatric UseNobelpharma USA, Inc. · 1999
  4. 5 generations backK992872 Branemark Bone-Anchored Hearing Aid (Baha) Cordelle IIEntific Medical Systems, Inc. · 1999
  5. 4 generations backK080363 Baha Cordelle IICochlear Bone Anchored Systems AB · 2008
  6. 3 generations backK090720 Cochlear Baha BP100Cochlear Bone Anchored Systems AB · 2009
  7. 2 generations backK132278 Cochlear Baha 4 Sound ProcessorCochlear Americas · 2013
  8. 1 generation backK142907 Baha 5 Sound ProcessorCochlear Americas · 2015 · Recalled
  9. This deviceK161123 Baha 5 Power Sound ProcessorCochlear Americas · 2016
  10. Descendant · cites it directly · 3 of its ownK202048 Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software…Cochlear Americas · 2021
  11. Descendant · 2 generations on · 1 of its ownK212136 Cochlear Baha 6 System, Cochlear Baha Fitting Software 6, Cochlear…Cochlear Americas · 2021
  12. Descendant · cites it directly · 0 of its ownK253431 Bone conduction Hearing Aid (BM100, BM300, BM310, SHOKZHEAR BM400…Shokz Health Global Limited · 2026
  13. Descendant · 3 generations on · 0 of its ownK254296 Ossiclear (Ossiclear System)Sounduct · 2026
  14. Descendant · 2 generations on · 0 of its ownK250215 Baha 7 Sound Processor; Baha Fitting Software 7 (P2121898); Baha…Cochlear · 2025

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2017: 12021: 22025: 12026: 2
2017high 2 (2021) · low 0 (2018)2026

Most influential descendants

Showing 5 of 6 · See all
  • K202048Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha…Cochlear Americas · 2021 · cites it directly3descendants
  • K212136Cochlear Baha 6 System, Cochlear Baha Fitting Software 6, Cochlear Baha Baha Smart AppCochlear Americas · 2021 · 2 generations on1descendant
  • K253431Bone conduction Hearing Aid (BM100, BM300, BM310, SHOKZHEAR BM400, SHOKZ BM400MN…Shokz Health Global Limited · 2026 · cites it directly0descendants
  • K254296Ossiclear (Ossiclear System)Sounduct · 2026 · 3 generations on0descendants
  • K250215Baha 7 Sound Processor; Baha Fitting Software 7 (P2121898); Baha Smart App (iOS)…Cochlear · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K861971Xomed Audiant Bone Conductor W/Improved AA CoilXomed, Inc.1986—
−7K955713Nobelpharma Bone Anchored Hearing AidNobelpharma USA, Inc.1996—
−6K984162Branemark Bone-Anchored Hearing Aid (Baha) System for Pediatric UseNobelpharma USA, Inc.1999—
−5K992872Branemark Bone-Anchored Hearing Aid (Baha) Cordelle IIEntific Medical Systems, Inc.1999—
−4K080363Baha Cordelle IICochlear Bone Anchored Systems AB2008—
−3K090720Cochlear Baha BP100Cochlear Bone Anchored Systems AB2009—
−2K132278Cochlear Baha 4 Sound ProcessorCochlear Americas2013—
−1K142907Baha 5 Sound ProcessorCochlear Americas20151
0 (this device)K161123Baha 5 Power Sound ProcessorCochlear Americas2016—
+1K202048Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6…Cochlear Americas2021—
+2K212136Cochlear Baha 6 System, Cochlear Baha Fitting Software 6, Cochlear Baha Baha…Cochlear Americas2021—
+1K253431Bone conduction Hearing Aid (BM100, BM300, BM310, SHOKZHEAR BM400, SHOKZ…Shokz Health Global Limited2026—
+3K254296Ossiclear (Ossiclear System)Sounduct2026—
+2K250215Baha 7 Sound Processor; Baha Fitting Software 7 (P2121898); Baha Smart App…Cochlear2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
199110
199310
199410
199510
199810
199910
200110
200210
200410
200810
201110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
202120
202510
202620
FIG. 1 — Lineage of K161123, 1986–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LXB? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new LXB device

  1. #1 K254296 Ossiclear (Ossiclear System)score 14.7 · 11 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K110996Baha 3 Power Sound Processor
Summary page 4
…21 CFR 874.3300, Class II Classification Panel Ear, Nose, and Throat Product Code: LXB 510(k): K110996 (Secondary) Trade/Proprietary Name: Baha 5 Sound Processor Common/Usual Name: Aud…
Cochlear Americas2011—
*K142907Baha 5 Sound Processor
Summary page 5
…21 CFR 874.3300, Class II Classification Panel Ear, Nose, and Throat Product Code: LXB 510(k): K142907 F. Purpose of Submission This submission requests the addition of the Baha 5 Power Sound Processor to the series of sound proce…
Cochlear Americas20151

Also cleared against K110996: 1 other device →

What descends from it? (6)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K202048Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha…Cochlear Americas20213
K253431Bone conduction Hearing Aid (BM100, BM300, BM310, SHOKZHEAR BM400, SHOKZ BM400MN…Shokz Health Global Limited20260
K171088Cochlear Baha SoundArcCochlear Americas20170

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 30 years and passes through 5 companies; a new generation was cleared every 2.9 years on median.
  • 1 of the 20 ancestors has a recall of any class.
  • Of its descendants, K202048 (Cochlear Americas, 2021) has gone furthest, with 3 descendants of its own.
  • 1 other device also cites its predicate K110996.

How does its category compare?

All LXB devices

LXB Hearing Aid, Bone Conduction: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.

FDA decisions per year · LXB

2in 2025

2008: 22009: 22010: 22011: 52012: 12013: 52015: 22016: 42017: 12018: 12019: 12021: 42025: 22026 (partial year): 4
2007high 5 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LXB

79in 2021

2011: 189 days median2013: 103 days median2016: 110 days median2021: 79 days median2026 (partial year): 164 days median
2007high 189 (2011) · low 79 (2021)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · LXB

1in 2018

2012: 52018: 1
2007high 5 (2012) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LXB

261in 2025

2007: 42008: 1102009: 762010: 912011: 1232012: 3462013: 6402014: 5452015: 8242016: 6922017: 3792018: 3362019: 4972020: 5472021: 4902022: 3872023: 3482024: 2322025: 261
2007high 824 (2015) · low 4 (2007)2025

MAUDE reports naming product code LXB, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—04
20082—0110
20092—076
20102—091
201151890123
20121—5346
201351030640
20140—0545
20152—0824
201641100692
20171—0379
20181—1336
20191—0497
20200—0547
20214790490
20220—0387
20230—0348
20240—0232
20252—0261
202641640—

What is it indicated for?

The Cochlear Baha® 5 Power Sound Processor is intended for the following patients and indications for use: Patient of any age for use with the Baha Softband or headband. Patients aged 5 and older for use with the Baha auditory osseointegrated implant system. Patients who have a conductive or mixed hearing loss and can still benefit from sound amplification. The pure tone average bone-conduction hearing threshold (measured at 0.5, 1, 2, and 3kHz) should…

Read the full statement (227 words)

The Cochlear Baha® 5 Power Sound Processor is intended for the following patients and indications for use:

Patient of any age for use with the Baha Softband or headband. Patients aged 5 and older for use with the Baha auditory osseointegrated implant system.

Patients who have a conductive or mixed hearing loss and can still benefit from sound amplification. The pure tone average bone-conduction hearing threshold (measured at 0.5, 1, 2, and 3kHz) should be better than or equal to 55 dB HL.

Bilateral fitting is intended for patients who meet the above criterion in both ears, with bilaterally symmetric moderate to severe conductive or mixed hearing loss. Symmetrical bone-conduction thresholds are defined as less than a 10 dB average difference between ears (measured at 0.5, 1, 2, and 3 kHz), or less than a 15 dB difference at individual frequencies.

Patients who suffer from unilateral sensorineural deafness in one ear with normal hearing in the other ear (i.e. Single-sided deadness: SSD). Normal hearing is defined as a pure tone average air-conduction hearing threshold (measured at 0.5, 1, 2, and 3 kHz) of better than or equal to 20 dB HL.

Baha for SSD is also indicated for any patient who is indicated for an air-conduction contralateral routing of signals (AC CROS) hearing aid, but who for some reason cannot or will not use an AC CROS.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K161123: Baha 5 Power Sound Processor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K161123

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026