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Corvus

FDA UDI

Class II (US FDA UDI)

by Hnm Total Recon Llc

Identity

Trade Name
CORVUS FDA UDI
Generic Name
Subtalar implant, non-bioabsorbable FDA UDI
Device Name
CORVUS Subtalar 12mm FDA UDI
Model / Reference
HTR-01-720625 FDA UDI
Description
CORVUS Subtalar 12mm FDA UDI

Identifiers

Catalog Number
HTR-01-720625 FDA UDI
Primary DI / UDI-DI
00841742100159 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Subtalar implant, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Subtalar implant, non-bioabsorbable

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

Similar devices

Also classified as Subtalar implant, non-bioabsorbable.

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 6f4dafba-829b-45be-b448-eea83d165ec2 34 fields · synced May 30, 2026