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CosmoLock Pedicle Screw System

FDA UDI

Class I (US FDA UDI)

by Kalitec Direct LLC

Identity

Trade Name
CosmoLock Pedicle Screw System FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Screwdriver Assembly, Tower Tab, Cannulated, SNI2 FDA UDI
Model / Reference
10-K01-7500 FDA UDI
Description
Screwdriver Assembly, Tower Tab, Cannulated, SNI2 FDA UDI

Identifiers

Primary DI / UDI-DI
B07310K0175000 FDA UDI
FDA Product Code
HXX FDA UDI
GMDN Term
Surgical screwdriver, reusable 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

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

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: Surgical screwdriver, reusable

CosmoLock Pedicle Screw System by Kalitec Direct LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kalitec Direct LLC

Sources (1)

  • FDA UDI ecc6bf8a-ef74-428d-9cf6-af5b57555601 33 fields · synced May 30, 2026