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ALPHALOK Plating System

FDA UDI

Class I (US FDA UDI)

by Vilex, Inc.

Identity

Trade Name
ALPHALOK Plating System FDA UDI
Generic Name
Fluted surgical drill bit, single-use FDA UDI
Device Name
RECON 2.7mm Over Drill FDA UDI
Model / Reference
TLD-27 FDA UDI
Description
RECON 2.7mm Over Drill FDA UDI

Identifiers

Catalog Number
TLD-27 FDA UDI
Primary DI / UDI-DI
00841731129635 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Fluted surgical drill bit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Fluted surgical drill bit, single-use

ALPHALOK Plating System by Vilex, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vilex, Inc.

Sources (1)

  • FDA UDI 2108b262-5b09-4835-80e2-5d6b01d0d25d 34 fields · synced Jun 8, 2026