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Vilex Plate Screw

FDA UDI

Class II (US FDA UDI)

by Vilex, Inc.

Identity

Trade Name
Vilex Plate Screw FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable, non-sterile FDA UDI
Device Name
Screw, Plate Cann. Non-Lkng 3.0x12mm_Ti L.Blue FDA UDI
Model / Reference
FT30-12T-11 FDA UDI
Description
Screw, Plate Cann. Non-Lkng 3.0x12mm_Ti L.Blue FDA UDI

Identifiers

Primary DI / UDI-DI
00841731107497 FDA UDI
510(k) Number
K041287 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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

No

FDA UDI

Lot / Batch Number

Yes

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: Orthopaedic fixation plate, non-bioabsorbable, non-sterile

Vilex Plate Screw by Vilex, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vilex, Inc.

Sources (1)

  • FDA UDI 4bf0623f-a523-473b-bfdf-c3a8cd5a00db 34 fields · synced May 31, 2026