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Zekrya Small Arc

FDA UDI

Class I (US FDA UDI)

by DMG America LLC

Identity

Trade Name
Zekrya Small Arc FDA UDI
Generic Name
Gingival retraction kit FDA UDI
Device Name
Zekrya Small Arc (bag of 10) to be used with the Zekrya Gingival Protector FDA UDI
Model / Reference
003-61097 FDA UDI
Description
Zekrya Small Arc (bag of 10) to be used with the Zekrya Gingival Protector FDA UDI

Identifiers

Catalog Number
003-61097 FDA UDI
Primary DI / UDI-DI
D033003610971 FDA UDI
FDA Product Code
BRW FDA UDI
GMDN Term
Gingival retraction kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5820 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Gingival retraction kit

Zekrya Small Arc by DMG America LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gingival retraction kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DMG America LLC

Sources (1)

  • FDA UDI 425f33db-8ced-4702-8b2a-d80231f4300f 35 fields · synced Jun 8, 2026