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SciPharm NewCore, Core Build-Up Restorative Automix

FDA UDI

Class II (US FDA UDI)

by Scientific Pharmaceuticals, Inc.

Identity

Trade Name
SciPharm NewCore, Core Build-Up Restorative Automix FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Newcore - Light-Cured Core Build-Up Restoratives in Automix Cartridges, Paste. Carpule. Boxed. FDA UDI
Model / Reference
SP 51-302 CB FDA UDI
Description
Newcore - Light-Cured Core Build-Up Restoratives in Automix Cartridges, Paste. Carpule. Boxed. FDA UDI

Identifiers

Catalog Number
51-302 FDA UDI
Primary DI / UDI-DI
D801SP51302CB1 FDA UDI
510(k) Number
K810479 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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 composite resin

SciPharm NewCore, Core Build-Up Restorative Automix by Scientific Pharmaceuticals, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Dental composite resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI afdc0a4f-3b01-4060-822e-e7942c148ea6 37 fields · synced Jun 8, 2026