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ItsoClear

FDA UDI

Class I (US FDA UDI)

by Keystone Industries

Identity

Trade Name
ItsoClear FDA UDI
Generic Name
Denture clasp, polymer, preformed FDA UDI
Device Name
Clear Universal Clasps Samples FDA UDI
Model / Reference
1009150M FDA UDI
Description
Clear Universal Clasps Samples FDA UDI

Identifiers

Catalog Number
1009150M FDA UDI
Primary DI / UDI-DI
H6681009150M1 FDA UDI
FDA Product Code
EHP FDA UDI
GMDN Term
Denture clasp, polymer, preformed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3285 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Denture clasp, polymer, preformed

ItsoClear by Keystone Industries — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Denture clasp, polymer, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Keystone Industries

Sources (1)

  • FDA UDI 8a9bf2e7-9845-4ba6-b333-d7db51b77a46 35 fields · synced Jun 9, 2026