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7.0mm Drill, Cann, Hudson-Mod, 190mm

FDA UDI

Class I (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
7.0mm Drill, Cann, Hudson-Mod, 190mm FDA UDI
Generic Name
Cannulated surgical drill bit, single-use, non-sterile FDA UDI
Device Name
7.0mm Drill, Cann, Hudson-Mod, 190mm FDA UDI
Model / Reference
2004-0020 FDA UDI
Description
7.0mm Drill, Cann, Hudson-Mod, 190mm FDA UDI

Identifiers

Catalog Number
2004-0020 FDA UDI
Primary DI / UDI-DI
00816950027826 FDA UDI
510(k) Number
K170021 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Cannulated surgical drill bit, single-use, non-sterile 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

Dimensions & Sizes

Size
Length — 190 Millimeter FDA UDI
Outer Diameter — 7.0 Millimeter FDA UDI

Category: Cannulated surgical drill bit, single-use, non-sterile

7.0mm Drill, Cann, Hudson-Mod, 190mm by OsteoCentric Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cannulated surgical drill bit, single-use, non-sterile.

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 d8df1e63-eb8f-4a10-b510-6ffa6eb0c48b 37 fields · synced May 30, 2026