← Back to catalogue

Humeris Shoulder

FDA UDI

Class II (US FDA UDI)

by Fx Solutions

Identity

Trade Name
Humeris Shoulder FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
TRIAL DOUBLE TAPER +0 mm +/-3° FDA UDI
Model / Reference
902-0030 FDA UDI
Description
TRIAL DOUBLE TAPER +0 mm +/-3° FDA UDI

Identifiers

Catalog Number
902-0030 FDA UDI
Primary DI / UDI-DI
03701037304174 FDA UDI
510(k) Number
K163669 FDA UDI
FDA Product Code
HSD FDA UDI
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

No

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

No

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 surgical procedure kit, non-medicated, reusable

Humeris Shoulder by Fx Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic surgical procedure kit, non-medicated, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Fx Solutions

Sources (1)

  • FDA UDI 6a868720-6451-489f-9990-57a85b662eee 35 fields · synced Jun 7, 2026