VeriFIT Splint

FDA UDI

Class U (US FDA UDI)

by Whip-Mix Corp.

Identity

Trade Name: VeriFIT Splint FDA UDI
Generic Name: Dental appliance fabrication material, resin FDA UDI
Device Name: 3D printing Thermo adaptive Splint resin FDA UDI
Model / Reference: 71183 FDA UDI
Description: 3D printing Thermo adaptive Splint resin FDA UDI

Identifiers

Primary DI / UDI-DI: D040711830 FDA UDI
510(k) Number: K241729 FDA UDI
FDA Product Code: MQC FDA UDI
KMY FDA UDI
GMDN Term: Dental appliance fabrication material, resin FDA UDI

Classification

Device Class: U FDA UDI
Regulation Number: 872.5525 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Dental appliance fabrication material, resin

VeriFIT Splint by Whip-Mix Corp. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class U	Pending data

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Manufacturer

Manufacturer: Whip-Mix Corp.

Sources (1)

FDA UDI 425197f7-aec8-4a2e-8667-b17f68bba107 34 fields · synced Jun 6, 2026