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2.0 x 130mm Drill Bit Calibrated

FDA UDI

Class I (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
2.0 x 130mm Drill Bit Calibrated FDA UDI
Generic Name
Fluted surgical drill bit, reusable FDA UDI
Device Name
2.0 x 130mm Drill Bit Calibrated FDA UDI
Model / Reference
317-0020 FDA UDI
Description
2.0 x 130mm Drill Bit Calibrated FDA UDI

Identifiers

Catalog Number
317-0020 FDA UDI
Primary DI / UDI-DI
00816950029516 FDA UDI
510(k) Number
K210247 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Fluted surgical drill bit, 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

Dimensions & Sizes

Size
Outer Diameter — 2.0 Millimeter FDA UDI
Length — 130 Millimeter FDA UDI

Category: Fluted surgical drill bit, reusable

2.0 x 130mm Drill Bit Calibrated by OsteoCentric Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, 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 e6c808e9-b089-49be-8b96-de066a70c3c9 37 fields · synced Jun 8, 2026