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Nakoma

FDA UDI

Class I (US FDA UDI)

by Alliance Partners Llc

Identity

Trade Name
Nakoma FDA UDI
Generic Name
Manual orthopaedic bender, reusable FDA UDI
Device Name
Plate Bender Instrument FDA UDI
Model / Reference
3100T-1200 FDA UDI
Description
Plate Bender Instrument FDA UDI

Identifiers

Catalog Number
3100T-1200 FDA UDI
Primary DI / UDI-DI
M6863100T12000 FDA UDI
510(k) Number
K141993 FDA UDI
FDA Product Code
HXW FDA UDI
GMDN Term
Manual orthopaedic bender, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Manual orthopaedic bender, reusable

Nakoma by Alliance Partners Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual orthopaedic bender, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ed26538f-8995-4257-af3e-2af334b38a9a 36 fields · synced May 30, 2026