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UCAN Print Splint

FDA UDI

Class U (US FDA UDI)

by Pro3Dure Medical

Identity

Trade Name
UCAN Print Splint FDA UDI
Generic Name
Dental appliance fabrication material, resin FDA UDI
Device Name
UCAN Print Splint 1000g Transparent FDA UDI
Model / Reference
1000g ; Transparent FDA UDI
Description
UCAN Print Splint 1000g Transparent FDA UDI

Identifiers

Catalog Number
768486 FDA UDI
Primary DI / UDI-DI
EPRC768486 FDA UDI
510(k) Number
K231775 FDA UDI
FDA Product Code
MQC FDA UDI
GMDN Term
Dental appliance fabrication material, resin FDA UDI

Classification

Device Class
U 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

Yes

FDA UDI

Category: Dental appliance fabrication material, resin

UCAN Print Splint by Pro3Dure Medical — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pro3Dure Medical

Sources (1)

  • FDA UDI 6043f5b2-b6ac-4984-8850-21347211fe71 35 fields · synced Jun 8, 2026