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Equinoxe

FDA UDI

Class II (US FDA UDI)

by Exactech, Inc.

Identity

Trade Name
Equinoxe FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
REVERSE SHOULDER, REPLICATOR, HANDLE, MODULAR FDA UDI
Model / Reference
321-10-35 FDA UDI
Description
REVERSE SHOULDER, REPLICATOR, HANDLE, MODULAR FDA UDI

Identifiers

Catalog Number
321-10-35 FDA UDI
Primary DI / UDI-DI
10885862087263 FDA UDI
510(k) Number
K042021 FDA UDI
K102951 FDA UDI
K121067 FDA UDI
FDA Product Code
KWT FDA UDI
KWS FDA UDI
HSD FDA UDI
PHX FDA UDI
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3650 FDA UDI
888.3660 FDA UDI
888.3690 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 prosthesis implantation positioning instrument, reusable

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

Similar devices

Also classified as Orthopaedic prosthesis implantation positioning instrument, reusable.

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 5871d1e2-ec1b-4738-85a2-1c3b979e244a 35 fields · synced May 31, 2026