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The Cutting Edge System

FDA UDI

Class II (US FDA UDI)

by Flexbar Machine Corp.

Identity

Trade Name
The Cutting Edge System FDA UDI
Generic Name
Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI
Device Name
Disposable Tip, Curved Metz Scissor, Sterile Pkg Single FDA UDI
Model / Reference
91710 FDA UDI
Description
Disposable Tip, Curved Metz Scissor, Sterile Pkg Single FDA UDI

Identifiers

Catalog Number
91710 FDA UDI
Primary DI / UDI-DI
00842102104565 FDA UDI
510(k) Number
K103840 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

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: Endoscopic electrosurgical electrode, monopolar, single-use

The Cutting Edge System by Flexbar Machine Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical electrode, monopolar, single-use.

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 d597e194-c094-47cf-b447-fa0204ead8fb 35 fields · synced Jun 1, 2026