Alamo P, Alamo T

FDA UDI

Class I (US FDA UDI)

by Alliance Partners Llc

Identity

Trade Name: Alamo P, Alamo T FDA UDI
Generic Name: Bone file/rasp, manual, reusable FDA UDI
Device Name: Rasp Instrument, Angled FDA UDI
Model / Reference: 2100T-1301 FDA UDI
Description: Rasp Instrument, Angled FDA UDI

Identifiers

Catalog Number: 2100T-1301 FDA UDI
Primary DI / UDI-DI: M6862100T13010 FDA UDI
510(k) Number: K120401 FDA UDI
K122047 FDA UDI
K140303 FDA UDI
FDA Product Code: HTR FDA UDI
GMDN Term: Bone file/rasp, manual, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone file/rasp, manual, reusable

Alamo P, Alamo T by Alliance Partners Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K122047 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Alliance Partners Llc

Sources (1)

FDA UDI 9cde6cfb-1661-4a2d-8a78-f5a361387fe7 36 fields · synced May 30, 2026