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Open Wide

FDA UDI

Class I (US FDA UDI)

by Specialized Care Co Inc

Identity

Trade Name
OPEN WIDE FDA UDI
Generic Name
Seizure bite block FDA UDI
Device Name
Mouth Rest Thick FDA UDI
Model / Reference
OWDT FDA UDI
Description
Mouth Rest Thick FDA UDI

Identifiers

Catalog Number
OWDT FDA UDI
Primary DI / UDI-DI
00859938000206 FDA UDI
FDA Product Code
KBN FDA UDI
GMDN Term
Seizure bite block FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Seizure bite block

Open Wide by Specialized Care Co Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Seizure bite block.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eff211b7-c0c2-4f0a-b2e3-75b31e80a350 34 fields · synced May 30, 2026