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Medpor

FDA UDI

Class I (US FDA UDI)

by Stryker Leibinger

Identity

Trade Name
Medpor FDA UDI
Generic Name
Intranasal splint, non-biodegradable FDA UDI
Device Name
Nostril Retainer Asymmetric - R3-L2 FDA UDI
Model / Reference
92-7240-2 FDA UDI
Description
Nostril Retainer Asymmetric - R3-L2 FDA UDI

Identifiers

Catalog Number
92-7240-2 FDA UDI
Primary DI / UDI-DI
07613327292305 FDA UDI
510(k) Number
K981374 FDA UDI
FDA Product Code
LYA FDA UDI
GMDN Term
Intranasal splint, non-biodegradable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Dimensions & Sizes

Size
Length — 24.0 Millimeter FDA UDI
Width — 18.6 Millimeter FDA UDI

Category: Intranasal splint, non-biodegradable

Medpor by Stryker Leibinger — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intranasal splint, non-biodegradable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Leibinger

Sources (1)

  • FDA UDI d0f84ec7-43cf-48b1-8f00-d3e5622f1186 36 fields · synced Jun 6, 2026