← Back to catalogue

Affinity™ Inflex FS 120ml Cartridge

FDA UDI

Class II (US FDA UDI)

by Den-Mat Holdings, LLC

Identity

Trade Name
Affinity™ Inflex FS 120ml Cartridge FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
VPS Impression Material FDA UDI
Model / Reference
012406 FDA UDI
Description
VPS Impression Material FDA UDI

Identifiers

Catalog Number
012406 FDA UDI
Primary DI / UDI-DI
00359883001513 FDA UDI
510(k) Number
K053014 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

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

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 120 Milliliter FDA UDI

Category: Silicone dental impression material

Affinity™ Inflex FS 120ml Cartridge by Den-Mat Holdings, 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b64572a3-ff0c-4966-965d-d6113376642b 38 fields · synced Jun 9, 2026