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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
TURBO TORQUE Reciprocating Endo Set (Motor & 10:1 red angle W/ hand file TEP-Y head) FDA UDI
Model / Reference
TT-20KTEP FDA UDI
Description
TURBO TORQUE Reciprocating Endo Set (Motor & 10:1 red angle W/ hand file TEP-Y head) FDA UDI

Identifiers

Catalog Number
TT-20KTEP FDA UDI
Primary DI / UDI-DI
00810113690391 FDA UDI
510(k) Number
K051872 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

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

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

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 5a1aa2d4-888c-43ba-a02a-3465d55d7b4d 36 fields · synced Jun 1, 2026