Ibis

FDA UDI

Class II (US FDA UDI)

by Ortho Development Corp.

Identity

Trade Name: Ibis FDA UDI
Generic Name: Spinal bone screw, non-bioabsorbable FDA UDI
Device Name: Diameter 4.5 mm x 25 mm Cannulated Monoaxial Screw FDA UDI
Model / Reference: 752-4525-41A FDA UDI
Description: Diameter 4.5 mm x 25 mm Cannulated Monoaxial Screw FDA UDI

Identifiers

Primary DI / UDI-DI: 00822409021376 FDA UDI
510(k) Number: K142146 FDA UDI
FDA Product Code: NKB FDA UDI
MNI FDA UDI
MNH FDA UDI
GMDN Term: Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3070 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 4.5 Millimeter FDA UDI
Length — 25 Millimeter FDA UDI

Category: Spinal bone screw, non-bioabsorbable

Ibis by Ortho Development Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

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Sterile and Non Sterile Spinal System — Shandong Weigao Orthopaedic Device Company Limited. · Class IIb
OpenLoc-L Spinal Fixation System — L&K BIOMED CO. , LTD. · Class II
Sterile and Non Sterile Spinal System — Shandong Weigao Orthopaedic Device Company Limited. · Class IIb
AccelFix Spinal Fixation System (Sterile) — L&K Biomed · Class IIb
Proficient™ Posterior Cervical Spine System — Spine Wave, Inc. · Class II

Cleared under the same submission

K142146 also covers:

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 II	Pending data

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Manufacturer

Manufacturer: Ortho Development Corp.

Sources (1)

FDA UDI 7b4e485e-6234-40f5-abab-61aa6aed4908 36 fields · synced May 30, 2026