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Ruthless Spine Straight Probe

FDA UDI

Class II (US FDA UDI)

by Ruthless Spine

Identity

Trade Name
Ruthless Spine Straight Probe FDA UDI
Generic Name
Abdominal/ENT/orthopaedic surgical probe, reusable FDA UDI
Device Name
Ruthless Spine Straight Probe FDA UDI
Model / Reference
RJB-PRB1 FDA UDI
Description
Ruthless Spine Straight Probe FDA UDI

Identifiers

Primary DI / UDI-DI
G492RJBPRB10 FDA UDI
510(k) Number
DEN230012 FDA UDI
FDA Product Code
QWL FDA UDI
GMDN Term
Abdominal/ENT/orthopaedic surgical probe, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.4560 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

Category: Abdominal/ENT/orthopaedic surgical probe, reusable

Ruthless Spine Straight Probe by Ruthless Spine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Abdominal/ENT/orthopaedic surgical probe, reusable.

Cleared under the same submission

DEN230012 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ruthless Spine

Sources (1)

  • FDA UDI c94bd53c-fb65-48a7-a4f9-491dd2449142 34 fields · synced May 30, 2026