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VECTOR® Screw

FDA UDI

Class I (US FDA UDI)

by Scheu-Dental

Identity

Trade Name
VECTOR® Screw FDA UDI
Generic Name
Orthodontic palate expander screw, self-removable FDA UDI
Device Name
VECTOR® 200, standard expansion screw maxi 10.00 x 3.10 x 14.30 mm Expansion 7.5 mm FDA UDI
Model / Reference
2498.2 FDA UDI
Description
VECTOR® 200, standard expansion screw maxi 10.00 x 3.10 x 14.30 mm Expansion 7.5 mm FDA UDI

Identifiers

Primary DI / UDI-DI
J01824982 FDA UDI
FDA Product Code
DYJ FDA UDI
GMDN Term
Orthodontic palate expander screw, self-removable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic palate expander screw, self-removable

VECTOR® Screw by Scheu-Dental — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic palate expander screw, self-removable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Scheu-Dental

Sources (1)

  • FDA UDI b42170a7-6b2d-4f02-8399-f839650dfd5d 33 fields · synced May 30, 2026