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EnsoSleep

FDA UDI

Class II (US FDA UDI)

by Ensodata, Inc.

Identity

Trade Name
EnsoSleep FDA UDI
Generic Name
Sleep disorder interpretive software, professional-only FDA UDI
Model / Reference
7.0 FDA UDI

Identifiers

Primary DI / UDI-DI
00864458000414 FDA UDI
510(k) Number
K210034 FDA UDI
FDA Product Code
OLZ FDA UDI
GMDN Term
Sleep disorder interpretive software, professional-only FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Sleep disorder interpretive software, professional-only

EnsoSleep by Ensodata, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sleep disorder interpretive software, professional-only.

Cleared under the same submission

K210034 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ensodata, Inc.

Sources (1)

  • FDA UDI 092960a6-a0ff-4cb9-b6a8-e92521fb92d3 33 fields · synced May 30, 2026