← Back to catalogue

F6 SkyTaper

FDA UDI

Class I (US FDA UDI)

by Sure Dent Corporation

Identity

Trade Name
F6 SkyTaper FDA UDI
Generic Name
Synthetic gutta-percha FDA UDI
Device Name
Gutta Percha Points Taper .06, Size 20-30, 60/PK, mm marked, SB, 20-30/.06 FDA UDI
Model / Reference
GPF06 FDA UDI
Description
Gutta Percha Points Taper .06, Size 20-30, 60/PK, mm marked, SB, 20-30/.06 FDA UDI

Identifiers

Primary DI / UDI-DI
18809264298159 FDA UDI
FDA Product Code
EKM FDA UDI
GMDN Term
Synthetic gutta-percha FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3850 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Synthetic gutta-percha

F6 SkyTaper by Sure Dent Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic gutta-percha.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 7dbeade8-3e6e-4e73-878b-01d8791f9004 34 fields · synced Jun 6, 2026