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HybenX

FDA UDI

Class U (US FDA UDI)

by Bicon, Llc

Identity

Trade Name
HybenX FDA UDI
Generic Name
Root canal cleaning solution FDA UDI
Device Name
HybenX OTD Syringe (2-Pack) FDA UDI
Model / Reference
103-2001 FDA UDI
Description
HybenX OTD Syringe (2-Pack) FDA UDI

Identifiers

Catalog Number
103-2001 FDA UDI
Primary DI / UDI-DI
00813110027337 FDA UDI
510(k) Number
K123538 FDA UDI
FDA Product Code
KJJ FDA UDI
GMDN Term
Root canal cleaning solution FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Root canal cleaning solution

HybenX by Bicon, Llc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Root canal cleaning solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bicon, Llc

Sources (1)

  • FDA UDI c7b3a5eb-4435-4692-a1ea-9938aaf05523 36 fields · synced May 30, 2026