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Apnea Guard

FDA UDI

Class II (US FDA UDI)

by Advanced Brain Monitoring, Inc.

Identity

Trade Name
Apnea Guard FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
Apnea Guard Starter Kit 2L2M1H (V2) FDA UDI
Model / Reference
AG25-1012 FDA UDI
Description
Apnea Guard Starter Kit 2L2M1H (V2) FDA UDI

Identifiers

Primary DI / UDI-DI
00850015266041 FDA UDI
510(k) Number
K111110 FDA UDI
FDA Product Code
LRK FDA UDI
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5570 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Silicone dental impression material

Apnea Guard by Advanced Brain Monitoring, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 11c57c5a-5d26-488f-96b2-5a97de686a63 35 fields · synced Jun 8, 2026