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Endo-Chisel, with handle

FDA UDI

Class I (US FDA UDI)

by Joimax, Inc.

Identity

Trade Name
Endo-Chisel, with handle FDA UDI
Generic Name
Orthopaedic chisel FDA UDI
Device Name
Bone Ablating Instruments (Curettes, Dissectors and Chisels) are hand-held manual surgical instruments, used to dissect or scrape/chisel tissue from a bony or soft tissue structure during minimally invasive endoscopic spinal surgery. It is typically a long, rigid instrument constructed of medical-grade stainless steel whose distal end has one or more sharp edges in order to fulfill the intended function described above. This is a reusable device. FDA UDI
Model / Reference
TEC273715 FDA UDI
Description
Bone Ablating Instruments (Curettes, Dissectors and Chisels) are hand-held manual surgical instruments, used to dissect or scrape/chisel tissue from a bony or soft tissue structure during minimally invasive endoscopic spinal surgery. It is typically a long, rigid instrument constructed of medical-grade stainless steel whose distal end has one or more sharp edges in order to fulfill the intended function described above. This is a reusable device. FDA UDI

Identifiers

Primary DI / UDI-DI
04250337119630 FDA UDI
FDA Product Code
FZS FDA UDI
GMDN Term
Orthopaedic chisel 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic chisel

Endo-Chisel, with handle by Joimax, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic chisel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Joimax, Inc.

Sources (1)

  • FDA UDI a07cedb9-b610-4457-9ee5-7cccaab89f1b 33 fields · synced May 30, 2026