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SmartPractice

FDA UDI

Class II (US FDA UDI)

by Smart Health Llc

Identity

Trade Name
SmartPractice FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
S/P HIGH PERF VPS PUTTY F/S 300ML BASE/CAT #VP8008 FDA UDI
Model / Reference
SP697673 FDA UDI
Description
S/P HIGH PERF VPS PUTTY F/S 300ML BASE/CAT #VP8008 FDA UDI

Identifiers

Catalog Number
SP697673 FDA UDI
Primary DI / UDI-DI
D766SP6976731 FDA UDI
510(k) Number
K801380 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

No

FDA UDI

Category: Silicone dental impression material

SmartPractice by Smart Health Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smart Health Llc

Sources (1)

  • FDA UDI 3df7d77c-7037-4845-8fb0-4633f18aec81 36 fields · synced Jun 8, 2026