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Ethox Medical

FDA UDI

Class II (US FDA UDI)

by Ethox Medical, Llc

Identity

Trade Name
Ethox Medical FDA UDI
Generic Name
Seizure bite block FDA UDI
Device Name
Bite Block FDA UDI
Model / Reference
950094201 FDA UDI
Description
Bite Block FDA UDI

Identifiers

Primary DI / UDI-DI
10889483150030 FDA UDI
510(k) Number
K921946 FDA UDI
FDA Product Code
JXL FDA UDI
GMDN Term
Seizure bite block FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5070 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Seizure bite block

Ethox Medical by Ethox Medical, Llc — Class II — 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

Manufacturer
Ethox Medical, Llc

Sources (1)

  • FDA UDI 2d975c30-d69f-48f4-a1be-0eb1d632dd6a 36 fields · synced May 30, 2026