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Imalac, Inc.

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Imalac, Inc. is a medical device manufacturer, with 71 devices listed in FDA GUDID (FDA Class I) as of 14 Nov 2026.

Devices
71

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • FDA GUDID 71
Device classes
  • FDA Class I 71
Identifiers
  • DUNS 081299239

What Imalac, Inc. makes

IMALAC, Inc. manufactures electric breast pumps, including wearable devices like the Nurture Bra and compression pads designed to support lactation and milk expression. These products are intended for use by breastfeeding individuals to facilitate hands-free milk removal and comfort during use.

The company’s devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue71

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Company details

DUNS number
081299239

Frequently asked questions

How many devices does IMALAC, INC. have in the registry?

The registry currently lists 71 devices for IMALAC, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list IMALAC, INC.'s devices?

Among its 50 most recently registered devices, IMALAC, INC. has devices listed in FDA GUDID (50 devices).

What risk classes do IMALAC, INC.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for IMALAC, INC.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from IMALAC, INC. in the registry?

The most recently registered devices listed for IMALAC, INC. include Nurture Bra BR-0DD-40-NU, Nurture Bra BR-0DD-36-NU, Nurture Compression Pad CP-00L-00-NU-L and Nurture Compression Pad CP-00L-00-BL-R.

Generated automatically from registry data and not verified by a human reviewer.