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GlasSpan Flexible Ceramic Bonding Rope Small Refill

FDA UDI

Class II (US FDA UDI)

by Practicon, Inc.

Identity

Trade Name
GlasSpan Flexible Ceramic Bonding Rope Small Refill FDA UDI
Generic Name
Dental reinforcing fibre FDA UDI
Model / Reference
SMALL ROPE FDA UDI

Identifiers

Catalog Number
701722 S FDA UDI
Primary DI / UDI-DI
10723896011772 FDA UDI
510(k) Number
K922673 FDA UDI
FDA Product Code
ELS FDA UDI
GMDN Term
Dental reinforcing fibre FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3890 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental reinforcing fibre

GlasSpan Flexible Ceramic Bonding Rope Small Refill by Practicon, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental reinforcing fibre.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Practicon, Inc.

Sources (1)

  • FDA UDI 6c2a945c-580e-4412-af13-1dd2c0d31e1e 34 fields · synced May 30, 2026