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Equinoxe

FDA UDI

Class II (US FDA UDI)

by Exactech, Inc.

Identity

Trade Name
Equinoxe FDA UDI
Generic Name
Orthopaedic fixation implant alignment tool FDA UDI
Device Name
REPLICATOR ALIGNMENT HDL FDA UDI
Model / Reference
301-16-41 FDA UDI
Description
REPLICATOR ALIGNMENT HDL FDA UDI

Identifiers

Catalog Number
301-16-41 FDA UDI
Primary DI / UDI-DI
10885862580498 FDA UDI
510(k) Number
K042021 FDA UDI
K102951 FDA UDI
K121067 FDA UDI
FDA Product Code
KWS FDA UDI
HSD FDA UDI
KWT FDA UDI
PHX FDA UDI
GMDN Term
Orthopaedic fixation implant alignment tool FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
888.3690 FDA UDI
888.3650 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: Orthopaedic fixation implant alignment tool

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

Similar devices

Also classified as Orthopaedic fixation implant alignment tool.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Exactech, Inc.

Sources (1)

  • FDA UDI 0caf04eb-e1f6-4e7a-b761-24b3cddb5570 35 fields · synced Jun 8, 2026