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Natural Extensions

FDA UDI

Class I (US FDA UDI)

by Benco Dental Supply Co.

Identity

Trade Name
NATURAL EXTENSIONS FDA UDI
Generic Name
Polychloroprene examination/treatment glove, non-powdered FDA UDI
Model / Reference
5942-732 FDA UDI

Identifiers

Primary DI / UDI-DI
00366975065292 FDA UDI
FDA Product Code
LZA FDA UDI
GMDN Term
Polychloroprene examination/treatment glove, non-powdered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Polychloroprene examination/treatment glove, non-powdered

Natural Extensions by Benco Dental Supply Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polychloroprene examination/treatment glove, non-powdered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4529531f-7f6c-4651-8344-e982463b1758 32 fields · synced Jun 1, 2026