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I-SIL Bite Registration Fast Set

FDA UDI

Class II (US FDA UDI)

by Spident Co., Ltd.

Identity

Trade Name
I-SIL Bite Registration Fast Set FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
Vinyl Polysiloxane Impression Material FDA UDI
Model / Reference
102-0101 FDA UDI
Description
Vinyl Polysiloxane Impression Material FDA UDI

Identifiers

Primary DI / UDI-DI
08809262959888 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Silicone dental impression material

I-SIL Bite Registration Fast Set by Spident Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spident Co., Ltd.

Sources (1)

  • FDA UDI 38f899ad-a5bf-40be-8f45-a8e2ce00325c 33 fields · synced May 30, 2026