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Rogue

FDA UDI

Class II (US FDA UDI)

by Life Spine, Inc.

Identity

Trade Name
Rogue FDA UDI
Generic Name
Orthopaedic bone pin, non-bioabsorbable FDA UDI
Device Name
Large Hammertoe Driver, 2.9mm Diameter FDA UDI
Model / Reference
154-456 FDA UDI
Description
Large Hammertoe Driver, 2.9mm Diameter FDA UDI

Identifiers

Catalog Number
154-456 FDA UDI
Primary DI / UDI-DI
00190837069919 FDA UDI
510(k) Number
K171448 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic bone pin, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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: Orthopaedic bone pin, non-bioabsorbable

Rogue by Life Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone pin, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Life Spine, Inc.

Sources (1)

  • FDA UDI 86a06d29-1fdf-4e07-b10f-61a5ddb1e1a8 35 fields · synced Jun 8, 2026