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Orocare Aspire Suction Toothbrush

FDA UDI

Class II (US FDA UDI)

by Intersurgical Incorporated

Identity

Trade Name
OROCARE ASPIRE SUCTION TOOTHBRUSH FDA UDI
Generic Name
Oral care kit, single-use FDA UDI
Device Name
OROCARE ASPIRE SUCTION TOOTHBRUSH FDA UDI
Model / Reference
3016000 FDA UDI
Description
OROCARE ASPIRE SUCTION TOOTHBRUSH FDA UDI

Identifiers

Primary DI / UDI-DI
05030267120581 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Oral care kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Oral care kit, single-use

Orocare Aspire Suction Toothbrush by Intersurgical Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oral care kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Intersurgical Incorporated

Sources (1)

  • FDA UDI 4a1c09b1-e6f8-4f50-b7b7-554aab26b855 34 fields · synced May 30, 2026