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iSmile

FDA UDI

Class II (US FDA UDI)

by Ismile Dental Products Inc.

Identity

Trade Name
iSmile FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
Sterilization Pouch 7-1/2" x 13" FDA UDI
Model / Reference
45-2508 FDA UDI
Description
Sterilization Pouch 7-1/2" x 13" FDA UDI

Identifiers

Catalog Number
45-2508 FDA UDI
Primary DI / UDI-DI
00816419020399 FDA UDI
510(k) Number
K172280 FDA UDI
FDA Product Code
FRG FDA UDI
GMDN Term
Sterilization packaging, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sterilization packaging, single-use

iSmile by Ismile Dental Products Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sterilization packaging, single-use.

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 038edc49-e645-4041-b0f0-9ccdc4d5e70b 36 fields · synced May 30, 2026