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Vector R&D, Inc

FDA UDI

Class I (US FDA UDI)

by Vector R&D, Inc.

Identity

Trade Name
Vector R&D, Inc FDA UDI
Generic Name
Dental delivery system instrument unit, pneumatic FDA UDI
Device Name
VECTOR MICROLite Super Mini Prophy Handpiece FDA UDI
Model / Reference
ML500 FDA UDI
Description
VECTOR MICROLite Super Mini Prophy Handpiece FDA UDI

Identifiers

Catalog Number
ML500 FDA UDI
Primary DI / UDI-DI
00810113690315 FDA UDI
510(k) Number
K022535 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Dental delivery system instrument unit, pneumatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 FDA UDI
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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Dental delivery system instrument unit, pneumatic

Vector R&D, Inc by Vector R&D, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental delivery system instrument unit, pneumatic.

Cleared under the same submission

K022535 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vector R&D, Inc.

Sources (1)

  • FDA UDI f4974d1f-50f7-4229-8ab5-8cea4092f860 36 fields · synced May 31, 2026