International Medical Devices Database

Manufacturer Address
Miramar Labs, Inc., 445 Indio Way, Sunnyvale CA 94085-4203
Manufacturer Parent Company (2017)
Sientra Inc.
Source
USFDA
1 Event
- Recall of MiraDry System

One device in the database

MiraDry System

Model / Serial
Serial numbers: 10H0158, 10H0160, 10H0161, 10H0167, 10H0172, 10H0185, 10H0193, 11H0035.
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
International only: Japan
Product Description
MiraDry System consisting of the DTS3000 Console, MiraDry Handpiece || (MD3001-HP), the miraDry biotip and the miraDry Treatment Template system. || Miramar Labs, Inc. || 445 Indio Way || Sunnyvale, CA 94085 || Intended use: Treatment of primary axillary hyperhidrosis.

One manufacturer with a similar name

Learn more about the data here

Miramar Labs, Inc.

Manufacturer Address
Miramar Labs, Inc., 2790 Walsh Ave, Santa Clara CA 95051-0963
Manufacturer Parent Company (2017)
Sientra Inc.
Source
USFDA

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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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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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