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Bioclear

FDA UDI

by Bioclear Matrix Systems, LLC

Identity

Trade Name
Bioclear FDA UDI
Generic Name
Dental abrasive air jet system handpiece FDA UDI
Device Name
Convenience kit of blaster, powder, and disclosing solution. FDA UDI
Model / Reference
Blaster FDA UDI
Description
Convenience kit of blaster, powder, and disclosing solution. FDA UDI

Identifiers

Primary DI / UDI-DI
D9494150112 FDA UDI
GMDN Term
Dental abrasive air jet system handpiece FDA UDI

Classification

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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental abrasive air jet system handpiece

Bioclear by Bioclear Matrix Systems, LLC — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental abrasive air jet system handpiece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bioclear Matrix Systems, LLC

Sources (1)

  • FDA UDI 3b78eae5-fc78-4963-8655-e13b6d736205 33 fields · synced Jun 1, 2026