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Fixation Button-Oblong

FDA UDI

Class II (US FDA UDI)

by Dunamis Medical LLC

Identity

Trade Name
Fixation Button-Oblong FDA UDI
Generic Name
Orthopaedic fixation suture button FDA UDI
Device Name
Fixation Button-Oblong FDA UDI
Model / Reference
AB-6100 FDA UDI
Description
Fixation Button-Oblong FDA UDI

Identifiers

Catalog Number
AB-6100 FDA UDI
Primary DI / UDI-DI
00850052601195 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic fixation suture button

Fixation Button-Oblong 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 52cc1613-5a3b-4dfa-a5a9-1aff9b1829da 36 fields · synced May 30, 2026