FlexiProp Reusable Mouth Prop 2 PK Medium

FDA UDI

Class I (US FDA UDI)

by Practicon, Inc.

Identity

Trade Name: FlexiProp Reusable Mouth Prop 2 PK Medium FDA UDI
Generic Name: Mouth gag, non-adjustable FDA UDI
Device Name: Reusable supportive mouth prop to keep patients mouth open. Ridged Bite Channels and floss eyelets ensure safety. 2 pack. Medium size FDA UDI
Model / Reference: 7158910 M FDA UDI
Description: Reusable supportive mouth prop to keep patients mouth open. Ridged Bite Channels and floss eyelets ensure safety. 2 pack. Medium size FDA UDI

Identifiers

Catalog Number: 7158910 M FDA UDI
Primary DI / UDI-DI: 00723896020234 FDA UDI
FDA Product Code: BRW FDA UDI
GMDN Term: Mouth gag, non-adjustable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

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Expiration Date

FDA UDI

Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Mouth gag, non-adjustable

FlexiProp Reusable Mouth Prop 2 PK Medium by Practicon, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Practicon, Inc.

Sources (1)

FDA UDI 4ef79c32-053d-415e-aa91-d8cebc7837b3 34 fields · synced Jun 6, 2026