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Chairside

FDA UDI

Class I (US FDA UDI)

by Zest Anchors, LLC

Identity

Trade Name
CHAIRSIDE FDA UDI
Generic Name
Gingiva bleaching protector FDA UDI
Device Name
CHAIRSIDE Block Out Material FDA UDI
Model / Reference
09574 FDA UDI
Description
CHAIRSIDE Block Out Material FDA UDI

Identifiers

Primary DI / UDI-DI
00840481122132 FDA UDI
FDA Product Code
EID FDA UDI
GMDN Term
Gingiva bleaching protector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 1.2 Milliliter FDA UDI

Category: Gingiva bleaching protector

Chairside by Zest Anchors, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gingiva bleaching protector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zest Anchors, LLC

Sources (1)

  • FDA UDI 2b22100c-0582-4d90-bd20-d8c0ef244985 35 fields · synced Jun 9, 2026