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Quattro

FDA UDI

Class II (US FDA UDI)

by PSM Medical Solutions

Identity

Trade Name
Quattro FDA UDI
Generic Name
Orthodontic anchoring screw FDA UDI
Device Name
quattro plus steril 2.0x15mm 22/28" FDA UDI
Model / Reference
ST-33-42215 FDA UDI
Description
quattro plus steril 2.0x15mm 22/28" FDA UDI

Identifiers

Primary DI / UDI-DI
04260482566128 FDA UDI
FDA Product Code
OAT FDA UDI
GMDN Term
Orthodontic anchoring screw FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthodontic anchoring screw

Quattro by PSM Medical Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic anchoring screw.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 59045e14-6f81-4e8b-8e11-beca76bda7ce 34 fields · synced May 30, 2026