International Medical Devices Database

Manufacturer Parent Company (2017)
AcuFocus Inc.
Source
AEMPSVFOI
2 Events
- Recall Or Safety Alert for KAMRATM corneal implant, model ACI 7000, catalog number 76125-05
- Recall Or Safety Alert for KAMRA corneal implant

2 devices in the database

KAMRATM corneal implant, model ACI 7000, catalog number 76125-05

Model / Serial

2 manufacturers with a similar name

Learn more about the data here

AcuFocus, Inc.

Manufacturer Address
AcuFocus, Inc., 32 Discovery Ste 200, Irvine CA 92618-3161
Manufacturer Parent Company (2017)
AcuFocus Inc.
Source
USFDA

AcuFocus, Inc.

Manufacturer Parent Company (2017)
AcuFocus Inc.
Source
SATP

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Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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AcuFocus, Inc.

2 devices in the database

KAMRATM corneal implant, model ACI 7000, catalog number 76125-05

KAMRA corneal implant

2 manufacturers with a similar name

AcuFocus, Inc.

AcuFocus, Inc.