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Verge

FDA UDI

Class I (US FDA UDI)

by Plastcare USA

Identity

Trade Name
Verge FDA UDI
Generic Name
Manual endodontic file/rasp, reusable FDA UDI
Device Name
Stainless Steel K File Size 6 Length 21 FDA UDI
Model / Reference
K2106 FDA UDI
Description
Stainless Steel K File Size 6 Length 21 FDA UDI

Identifiers

Primary DI / UDI-DI
D915K21061 FDA UDI
FDA Product Code
EKS FDA UDI
GMDN Term
Manual endodontic file/rasp, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Manual endodontic file/rasp, reusable

Verge by Plastcare USA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual endodontic file/rasp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Plastcare USA

Sources (1)

  • FDA UDI 20a1b951-4d66-4b6f-b816-bf306a6d97fb 33 fields · synced May 30, 2026