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Aurora Spine

FDA UDI

Class II (US FDA UDI)

by Aurora Spine, Inc.

Identity

Trade Name
Aurora Spine FDA UDI
Generic Name
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile FDA UDI
Device Name
ZIP ULTRA, SHORT COMPRESSOR FDA UDI
Model / Reference
ZIP FDA UDI
Description
ZIP ULTRA, SHORT COMPRESSOR FDA UDI

Identifiers

Catalog Number
001-303 FDA UDI
Primary DI / UDI-DI
B5210013030 FDA UDI
FDA Product Code
PEK FDA UDI
GMDN Term
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile

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

Similar devices

Also classified as Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aurora Spine, Inc.

Sources (1)

  • FDA UDI c67097eb-ec11-4e1c-a7c7-160b95011586 35 fields · synced May 31, 2026