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OsteoCentric Headless Compression System Drill Guide Percutaneous

FDA UDI

Class I (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
OsteoCentric Headless Compression System Drill Guide Percutaneous FDA UDI
Generic Name
Surgical drill guide, reusable FDA UDI
Device Name
Headless Compression System Drill Guide Percutaneous FDA UDI
Model / Reference
EX01-0008 FDA UDI
Description
Headless Compression System Drill Guide Percutaneous FDA UDI

Identifiers

Catalog Number
EX01-0008 FDA UDI
Primary DI / UDI-DI
00850015496301 FDA UDI
510(k) Number
K200259 FDA UDI
FDA Product Code
HTW 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

No

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

No

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

OsteoCentric Headless Compression System Drill Guide Percutaneous by OsteoCentric Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID

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 49c1d44f-6454-4c60-91f8-e0c3d51f8c0a 36 fields · synced May 30, 2026