Titan™

FDA UDI

Class I (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name: Titan™ FDA UDI
Generic Name: Cannulated surgical drill bit, reusable FDA UDI
Device Name: Titan™ Reverse Shoulder System The reamer guide body inserter/extractor knob is used to tighten or loosen the reamer guide body inserter/extractor. FDA UDI
Model / Reference: INS096004902 FDA UDI
Description: Titan™ Reverse Shoulder System The reamer guide body inserter/extractor knob is used to tighten or loosen the reamer guide body inserter/extractor. FDA UDI

Identifiers

Catalog Number: INS-0960-049-02 FDA UDI
Primary DI / UDI-DI: 10381780245865 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Cannulated 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

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Serial Number

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Expiration Date

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Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Cannulated surgical drill bit, reusable

Titan™ by Ascension Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Ascension Orthopedics, Inc.

Sources (1)

FDA UDI fc4949fa-54c6-4842-904c-36af49daa524 37 fields · synced May 30, 2026