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Ibis Xl

FDA UDI

Class II (US FDA UDI)

by Ortho Development Corp.

Identity

Trade Name
IBIS XL FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
Diameter 8.5 x 120 mm Cannulated Polyaxial Screw FDA UDI
Model / Reference
752-8512-57A FDA UDI
Description
Diameter 8.5 x 120 mm Cannulated Polyaxial Screw FDA UDI

Identifiers

Primary DI / UDI-DI
00822409034437 FDA UDI
FDA Product Code
NKB 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 8.5 Millimeter FDA UDI
Length — 120 Millimeter FDA UDI

Category: Spinal bone screw, non-bioabsorbable

Ibis Xl 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a08c91ec-a506-434e-9225-3b26fecc4d65 35 fields · synced May 31, 2026