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Piccolo Composite Plate System

FDA UDI

Class II (US FDA UDI)

by Carbofix Orthopedics Ltd

Identity

Trade Name
Piccolo Composite Plate System FDA UDI
Generic Name
Bone holding forceps FDA UDI
Device Name
Forceps for use with the Piccolo Composite Distal Radius, Distal Fibula and One-Third Tubular Plate Systems FDA UDI
Model / Reference
Forceps - Pointed Tip FDA UDI
Description
Forceps for use with the Piccolo Composite Distal Radius, Distal Fibula and One-Third Tubular Plate Systems FDA UDI

Identifiers

Catalog Number
PL921810 FDA UDI
Primary DI / UDI-DI
07290109339320 FDA UDI
510(k) Number
K102597 FDA UDI
K120409 FDA UDI
K160002 FDA UDI
FDA Product Code
KTT FDA UDI
HRS FDA UDI
GMDN Term
Bone holding forceps FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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: Bone holding forceps

Piccolo Composite Plate System by Carbofix Orthopedics Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone holding forceps.

Cleared under the same submission

K102597 also covers:

K120409 also covers:

K160002 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Carbofix Orthopedics Ltd

Sources (1)

  • FDA UDI c2bdc7bf-cc4e-4b43-9dcc-6ec3aa7720aa 36 fields · synced May 30, 2026