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NEXT Medium Spearmint Prophy Paste Box 200

FDA UDI

Class I (US FDA UDI)

by Preventech

Identity

Trade Name
NEXT Medium Spearmint Prophy Paste Box 200 FDA UDI
Generic Name
Dentifrice FDA UDI
Device Name
NEXT Medium Spearmint Prophy Paste Box of 200 2.0g prophy cup units for dental prophylaxis procedures FDA UDI
Model / Reference
220293 FDA UDI
Description
NEXT Medium Spearmint Prophy Paste Box of 200 2.0g prophy cup units for dental prophylaxis procedures FDA UDI

Identifiers

Catalog Number
220293 FDA UDI
Primary DI / UDI-DI
D024220293 FDA UDI
510(k) Number
K100539 FDA UDI
FDA Product Code
EJR FDA UDI
GMDN Term
Dentifrice FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6030 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

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: Dentifrice

NEXT Medium Spearmint Prophy Paste Box 200 by Preventech — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dentifrice.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Preventech

Sources (1)

  • FDA UDI 420587ff-2cf4-4967-aa71-2fda296d5d40 36 fields · synced May 30, 2026