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Salvation™

FDA UDI

Class I (US FDA UDI)

by Wright Medical Technology, Inc.

Identity

Trade Name
SALVATION™ FDA UDI
Generic Name
Orthopaedic implant aiming/guiding block, reusable FDA UDI
Device Name
Foot Positioner FDA UDI
Model / Reference
SEF99602 FDA UDI
Description
Foot Positioner FDA UDI

Identifiers

Catalog Number
SEF99602 FDA UDI
Primary DI / UDI-DI
00889797076876 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic implant aiming/guiding block, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic implant aiming/guiding block, reusable

Salvation™ by Wright Medical Technology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant aiming/guiding block, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 08ae2327-5b83-4f3c-898d-bf330a0f9b20 35 fields · synced Jun 8, 2026