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Korona

FDA UDI

Class II (US FDA UDI)

by Hnm Total Recon Llc

Identity

Trade Name
KORONA FDA UDI
Generic Name
Orthopaedic bone staple, non-adjustable FDA UDI
Device Name
KORONA Tri Staple - (L)12.5mm, 10mmx8mm FDA UDI
Model / Reference
HTR-01-820563 FDA UDI
Description
KORONA Tri Staple - (L)12.5mm, 10mmx8mm FDA UDI

Identifiers

Catalog Number
HTR-01-820563 FDA UDI
Primary DI / UDI-DI
00841742100708 FDA UDI
510(k) Number
K072298 FDA UDI
FDA Product Code
JDR FDA UDI
GMDN Term
Orthopaedic bone staple, non-adjustable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic bone staple, non-adjustable

Korona by Hnm Total Recon Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone staple, non-adjustable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hnm Total Recon Llc

Sources (1)

  • FDA UDI 163dce66-13c7-428d-bd2c-3856937a7064 35 fields · synced May 30, 2026