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2.5 Hex Driver Long

FDA UDI

Class I (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
2.5 Hex Driver Long FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
2.5 Hex Driver Long FDA UDI
Model / Reference
110104 FDA UDI
Description
2.5 Hex Driver Long FDA UDI

Identifiers

Catalog Number
110104 FDA UDI
Primary DI / UDI-DI
00816950028403 FDA UDI
510(k) Number
K152000 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

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: Surgical screwdriver, reusable

2.5 Hex Driver Long by OsteoCentric Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ecd17327-775d-4ab6-bfc9-dcee28e139b0 36 fields · synced May 30, 2026