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Advanced Bionics

Last updated May 23, 2026

Information

Country: US
Address: —
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FDA FEI Number: —
DUNS Number: —

Catalogue (1669)

Page 5 of 34

Device	Model / Reference	Registries	Class	Status
RF Cable	CI-5415-502	FDA UDI	Class III	Unknown
Slim HP AquaMic™	CI-5321-014	FDA UDI	Class III	Unknown
Naida CI Q70	CI-5245-190	FDA UDI	Class III	Unknown
HiFocus Electrode Forceps Kit	CI-4350-02	FDA UDI	Class III	Active
Slim HP 3D Magnet	CI-7525-005	FDA UDI	Class III	Unknown
Uhp 3d	CI-5316	FDA UDI	Class III	Unknown
BTE Cable	CI-5403-310	FDA UDI	Class III	Active
Neptune™ Covers	CI-7126-320	FDA UDI	Class III	Unknown
Power Adapter Cable	CI-7405-072	FDA UDI	Class III	Unknown
Slim HP	CI-5320-007	FDA UDI	Class III	Active
Naída™ CI M30 Sound Processor	CI-5294-130	FDA UDI	Class III	Unknown
RF Cable	CI-5415-301	FDA UDI	Class III	Unknown
Naída™ CI M90 Sound Processor	CI-5293-130	FDA UDI	Class III	Unknown
Neptune™ Cable for AquaMic™	CI-5414-501	FDA UDI	Class III	Active
MRI Antenna Coil Cover	CI-7521	FDA UDI	Class III	Unknown
Auria™ iConnect	CI-5751-100	FDA UDI	Class III	Unknown
Slim HP Standard Magnet	CI-7524-007	FDA UDI	Class III	Active
Slim HP Standard Magnet 1	CI-7524-001	FDA UDI	Class III	Active
Slim HP 3D Magnet 1	CI-7525-001	FDA UDI	Class III	Active
Neptune™ Cable for AquaMic™	CI-5414-201	FDA UDI	Class III	Active
Power Adapter Cable	CI-7405-040	FDA UDI	Class III	Active
CPI-3 BTE Programming Cable	CI-6407	FDA UDI	Class III	Unknown
AquaMic™ Color Caps	CI-7127-WHT	FDA UDI	Class III	Active
HiRes™ Ultra CI HiFocus™ SlimJ Electrode	CI-1600-05	FDA UDI	Class III	Unknown
UHP Color Cap	CI-7125-BLK	FDA UDI	Class III	Unknown
PowerCel™ 170	CI-5517-120	FDA UDI	Class III	Active
Naida CI Q70	CI-5245-120	FDA UDI	Class III	Active
Slim HP	CI-5323	FDA UDI	Class III	Unknown
Neptune™ Cable for UHP	CI-5413-306	FDA UDI	Class III	Unknown
Power Adapter Cable	CI-7405-082	FDA UDI	Class III	Unknown
Auria™ Direct Connect	CI-5840-120	FDA UDI	Class III	Active
RF Cable	CI-5415-501	FDA UDI	Class III	Active
Helix Cochleostomy Sizing Gauge	CI-4345	FDA UDI	Class III	Unknown
Auria™ External Magnet	CI-7510-920	FDA UDI	Class III	Unknown
UHP 3D Color Cap	CI-7129-220	FDA UDI	Class III	Active
HiRes™ Ultra Replacement Magnet	CI-1413	FDA UDI	Class III	Unknown
SoundWave™ Professional Suite Software	CI-6055-011	FDA UDI	Class III	Active
AquaMic™	CI-5306	FDA UDI	Class III	Active
Naida CI Q90 Acoustic Earhook	CI-5850-007	FDA UDI	Class III	Unknown
PowerCel™ 170	CI-5517-190	FDA UDI	Class III	Unknown
Slim HP Magnet Kit	CI-7528	FDA UDI	Class III	Active
Sky CI™ M90	CI-5295	FDA UDI	Class III	Active
CPI-3 Naida CI Programming Cable	CI-6405	FDA UDI	Class III	Active
M T-Mic™	CI-5837-100	FDA UDI	Class III	Active
Auria™ Headpiece	CI-5304-223	FDA UDI	Class III	Unknown
Power Adapter Cable	CI-7405-010	FDA UDI	Class III	Unknown
Sky CI™ M90	CI-5295	FDA UDI	Class III	Active
Neptune™ Cable for AquaMic™	CI-5414-506	FDA UDI	Class III	Active
Auria™ Standard Earhook	CI-5730-100	FDA UDI	Class III	Active
Naida CI Q90 Acoustic Earhook	CI-5850-005	FDA UDI	Class III	Unknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

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FDA Recalls (28)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Apr 30, 2026	Z-2283-2026	—	open, classified	Due to incorrect shelf-life expiration date.
Mar 23, 2026	Z-1950-2026	—	open, classified	The non-tamperproof battery door supplied with the sound processor fails to conform to IEC 60601-1-11:2015 by not requiring the use of a tool to replace the button/coin cell battery.
Nov 27, 2025	Z-1493-2026	—	open, classified	Behind-the-ear sound processer packaging label is different then included product.
Mar 5, 2025	Z-1813-2025	—	open, classified	Due to incorrect the battery charger being packaged and distributed. Product labeling does not match the intended product as specified.
Sep 26, 2020	Z-0486-2021	—	terminated	Mislabeling; It has been determined that some batteries were improperly labeled and may contain a different battery life than indicated.
Sep 26, 2020	Z-0487-2021	—	terminated	Mislabeling; It has been determined that some batteries were improperly labeled and may contain a different battery life than indicated.
Feb 17, 2020	Z-2033-2020	—	terminated	hearing performance degradation due to body-fluid entering the device.
Feb 17, 2020	Z-2032-2020	—	terminated	hearing performance degradation due to body-fluid entering the device.
Apr 4, 2019	Z-1441-2020	—	terminated	The manufacturer received complaints that customers were attempting to install the fitting software using the supplied USB drive, an error message was received, and installation failed. The failed installation has not impact to the current version of the software, and users are able to continue programming devices with the current software version.
Mar 18, 2019	Z-1259-2020	—	terminated	Three materials used in the makeup of the implant were mistakenly left off the list of bio-compatible materials in the firm's previously approved submission to the Pharmaceuticals and Medical Devices Agency (PMDA) of Japan.
Feb 6, 2019	Z-1083-2019	—	terminated	The sound processors were loaded with the incorrect firmware.
Feb 6, 2019	Z-1085-2019	—	terminated	The sound processors were loaded with the incorrect firmware.
Feb 6, 2019	Z-1084-2019	—	terminated	The sound processors were loaded with the incorrect firmware.
Jun 10, 2009	Z-2039-2009	—	terminated	The recall was initiated after Advanced Bionics became aware of fourteen (14) devices manufactured between May 27, 2005 and June 30, 2005 that are confirmed to have or potentially have an issue related to the internal magnet. These devices are were made with an internal magnet where the metal case surrounding the magnet was not properly welded. Patients with these devices may experience a decreas
Sep 22, 2008	Z-0271-2009	—	terminated	Since April 2004, 27 of 8,769 (0.31%) patients have reported receiving second degree burns in the area of charging and 3 of 8,769 (0.03%) patients have reported receiving third degree burns in the area of charging while using Charger 1 .0. Some of these events were the direct result of the patient disregarding the instructions for use, such as sleeping with the Charger on or placing it directly on
Jul 24, 2008	Z-0958-2009	—	terminated	Mistuned headpiece - Advanced Bionics recently became aware of a tuning issue with some Platinum Series and S-Series headpieces shipped from May 2007 through April 2008. Tuning refers to the process through which the headpiece's communication frequency is adjusted to match that of the internal device. Potential clinical symptoms include: -No lock -Intermittent lock -Implant locks, but can
Jul 24, 2008	Z-0956-2009	—	terminated	Mistuned headpiece - Advanced Bionics recently became aware of a tuning issue with some Platinum Series and S-Series headpieces shipped from May 2007 through April 2008. Tuning refers to the process through which the headpiece's communication frequency is adjusted to match that of the internal device. Potential clinical symptoms include: -No lock -Intermittent lock -Implant locks, but cann
Jul 24, 2008	Z-0957-2009	—	terminated	Mistuned headpiece - Advanced Bionics recently became aware of a tuning issue with some Platinum Series and S-Series headpieces shipped from May 2007 through April 2008. Tuning refers to the process through which the headpiece's communication frequency is adjusted to match that of the internal device. Potential clinical symptoms include: -No lock -Intermittent lock -Implant locks, but can
Jul 24, 2008	Z-0959-2009	—	terminated	Mistuned headpiece - Advanced Bionics recently became aware of a tuning issue with some Platinum Series and S-Series headpieces shipped from May 2007 through April 2008. Tuning refers to the process through which the headpiece's communication frequency is adjusted to match that of the internal device. Potential clinical symptoms include: -No lock -Intermittent lock -Implant locks, but cann
Oct 5, 2007	Z-0960-2008	—	terminated	Incorrect Data -- Corruption of internal memory component results in an inability for the physician to reprogram the IPG with firmware version prior to Revision 3.02. When this occurs, the IPG will report an error code of "10h0" or "00h0" through the Remote Control. Under this condition, the IPG will cease to log in some data that could be used for informational purposes. ** It should be noted t
Oct 5, 2007	Z-0961-2008	—	terminated	Incorrect Data -- Corruption of internal memory component results in an inability for the physician to reprogram the IPG with firmware version prior to Revision 3.02. When this occurs, the IPG will report an error code of "10h0" or "00h0" through the Remote Control. Under this condition, the IPG will cease to log in some data that could be used for informational purposes. ** It should be noted t
Aug 3, 2007	Z-0055-2008	—	terminated	Mislabeled: Product labeled with the incorrect shelf-life information.
Jan 30, 2007	Z-0700-2007	—	terminated	The Precision Implantable Pulse Generator with firmware Revision 3.01 incorrectly reports an error condition for a valid output from its self internal check.
Nov 11, 2004	Z-0396-05	—	terminated	A burn injury was sustained by a patient that did not follow the directions for use and also slept while charging the unit.
Sep 27, 2004	Z-0045-05	—	terminated	All unimplanted CLARION and HiResolution cochlear implants due to the potential presence of moisture in the internal circuitry, which can cause the device to stop functioning.
Sep 27, 2004	Z-0044-05	—	terminated	All unimplanted CLARION and HiResolution cochlear implants due to the potential presence of moisture in the internal circuitry, which can cause the device to stop functioning.
Sep 27, 2004	Z-0046-05	—	terminated	All unimplanted CLARION and HiResolution cochlear implants due to the potential presence of moisture in the internal circuitry, which can cause the device to stop functioning.
Jul 27, 2004	Z-1332-04	—	terminated	Battery pack may overheat and cause patient burns.