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SureMAX-SA

FDA UDI

Class II (US FDA UDI)

by Additive Implants, Inc.

Identity

Trade Name
SureMAX-SA FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
SureMAX-SA — 14° Medium 8 FDA UDI
Model / Reference
1 FDA UDI
Description
SureMAX-SA — 14° Medium 8 FDA UDI

Identifiers

Catalog Number
1022-14141608 FDA UDI
Primary DI / UDI-DI
00817662025445 FDA UDI
510(k) Number
K211111 FDA UDI
FDA Product Code
OVE FDA UDI
GMDN Term
Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Metallic spinal interbody fusion cage

SureMAX-SA by Additive Implants, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a64d9c71-5d4f-47a4-b986-dbab8f862a84 36 fields · synced May 30, 2026