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Hallux Guide

FDA UDI

Class II (US FDA UDI)

by Dunamis Medical LLC

Identity

Trade Name
Hallux Guide FDA UDI
Generic Name
Orthopaedic fixation suture button FDA UDI
Device Name
Hallux Guide FDA UDI
Model / Reference
DU1000 FDA UDI
Description
Hallux Guide FDA UDI

Identifiers

Catalog Number
DU1000 FDA UDI
Primary DI / UDI-DI
00850052601072 FDA UDI
510(k) Number
K191319 FDA UDI
FDA Product Code
MBI FDA UDI
HTN FDA UDI
GMDN Term
Orthopaedic fixation suture button FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic fixation suture button

Hallux Guide by Dunamis Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation suture button.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dunamis Medical LLC

Sources (1)

  • FDA UDI 0729bb5a-4f0d-4b5f-8ec3-785ab454bdf5 36 fields · synced Jun 8, 2026