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C.i.™

FDA UDI

Class I (US FDA UDI)

by Parkell, Inc.

Identity

Trade Name
C.I.™ FDA UDI
Generic Name
Root canal post kit FDA UDI
Device Name
Medium C.I.™ White Fiber Post Refills (Pkg. of 20 Posts) FDA UDI
Model / Reference
S093 FDA UDI
Description
Medium C.I.™ White Fiber Post Refills (Pkg. of 20 Posts) FDA UDI

Identifiers

Catalog Number
S093 FDA UDI
Primary DI / UDI-DI
00810000526222 FDA UDI
FDA Product Code
ELR FDA UDI
GMDN Term
Root canal post kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3810 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

Yes

FDA UDI

Lot / Batch Number

No

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: Root canal post kit

C.i.™ by Parkell, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Root canal post kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Parkell, Inc.

Sources (1)

  • FDA UDI 8c9955c2-f6ab-45b8-88aa-5508f264bd49 35 fields · synced Jun 8, 2026