← Back to catalogue

everStick®

FDA UDI

Class II (US FDA UDI)

by Gc America Inc.

Identity

Trade Name
everStick® FDA UDI
Generic Name
Dental restoration retention pin FDA UDI
Device Name
everStick® PERIO 2 x 12 cm fiber bundles FDA UDI
Model / Reference
900822 FDA UDI
Description
everStick® PERIO 2 x 12 cm fiber bundles FDA UDI

Identifiers

Catalog Number
900822 FDA UDI
Primary DI / UDI-DI
J0229008221 FDA UDI
510(k) Number
K030072 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Dental restoration retention pin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental restoration retention pin

everStick® by Gc America Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental restoration retention pin.

Cleared under the same submission

K030072 also covers:

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

Manufacturer
Gc America Inc.

Sources (1)

  • FDA UDI 7b09701e-bdea-478c-b9bd-bcf769d76938 37 fields · synced May 29, 2026