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Fiber Force

FDA UDI

Class II (US FDA UDI)

by Synca Marketing Inc

Identity

Trade Name
FIBER FORCE FDA UDI
Generic Name
Dental reinforcing fibre FDA UDI
Device Name
WHITE BRAIDED ROPE 2MM (2-150MM) FDA UDI
Model / Reference
FF08011 FDA UDI
Description
WHITE BRAIDED ROPE 2MM (2-150MM) FDA UDI

Identifiers

Primary DI / UDI-DI
66714700001118 FDA UDI
510(k) Number
K102207 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Dental reinforcing fibre FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 FDA UDI
Commercial Distribution
Not 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

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

Dimensions & Sizes

Size
Length — 150 Millimeter FDA UDI

Fiber Force by Synca Marketing Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K102207 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synca Marketing Inc

Sources (1)

  • FDA UDI a4e3e6ad-af00-4423-acd2-b11a04867d8e 38 fields · synced Jun 8, 2026