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2.5mm Hex Driver Sleeve

FDA UDI

Class I (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
2.5mm Hex Driver Sleeve FDA UDI
Generic Name
Surgical drill guide, reusable FDA UDI
Device Name
2.5mm Hex Driver Sleeve FDA UDI
Model / Reference
110701 FDA UDI
Description
2.5mm Hex Driver Sleeve FDA UDI

Identifiers

Catalog Number
110701 FDA UDI
Primary DI / UDI-DI
00816950028571 FDA UDI
510(k) Number
K152000 FDA UDI
FDA Product Code
HXX FDA UDI
GMDN Term
Surgical drill guide, 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 drill guide, reusable

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

Similar devices

Also classified as Surgical drill guide, 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 8d7ebccf-caed-411b-9462-e2142226397c 36 fields · synced May 29, 2026