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SMR Shoulder

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
SMR Shoulder FDA UDI
Generic Name
Glenoid orthopaedic reamer FDA UDI
Device Name
Bone Graft Instrument Set - SMALL-R/SMALL Glenoid Flat Reamer FDA UDI
Model / Reference
Bone Graft Instrument Set FDA UDI
Description
Bone Graft Instrument Set - SMALL-R/SMALL Glenoid Flat Reamer FDA UDI

Identifiers

Catalog Number
9013.75.401 FDA UDI
Primary DI / UDI-DI
08033390108768 FDA UDI
510(k) Number
K161120 FDA UDI
FDA Product Code
PHX FDA UDI
KWT FDA UDI
KWS FDA UDI
GMDN Term
Glenoid orthopaedic reamer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 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: Glenoid orthopaedic reamer

SMR Shoulder by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glenoid orthopaedic reamer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI c7a76264-3036-48bd-884f-f4ec7a6a5a34 36 fields · synced Jun 8, 2026