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ORIA™ Spinal Clip System

FDA UDI

Class II (US FDA UDI)

by Choicespine, LP

Identity

Trade Name
ORIA™ Spinal Clip System FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Device Name
SCS,SCREW,POLYAXIAL,9.5X35 FDA UDI
Model / Reference
2T10-BD935 FDA UDI
Description
SCS,SCREW,POLYAXIAL,9.5X35 FDA UDI

Identifiers

Primary DI / UDI-DI
00840996121521 FDA UDI
510(k) Number
K023994 FDA UDI
FDA Product Code
MNH FDA UDI
MNI FDA UDI
KWP FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
888.3050 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
Length — 35 Millimeter FDA UDI
Outer Diameter — 9.5 Millimeter FDA UDI

Category: Bone-screw internal spinal fixation system, non-sterile

ORIA™ Spinal Clip System by Choicespine, LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Choicespine, LP

Sources (1)

  • FDA UDI 25a65c96-7165-448e-a4a9-3608a9410953 36 fields · synced May 31, 2026