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Waterpik Key-To Alginate Impression Material

FDA UDI

Class II (US FDA UDI)

by Water Pik, Inc.

Identity

Trade Name
Waterpik Key-To Alginate Impression Material FDA UDI
Generic Name
Alginate dental impression material FDA UDI
Device Name
Regular Body, Regular Set FDA UDI
Model / Reference
013111-000 FDA UDI
Description
Regular Body, Regular Set FDA UDI

Identifiers

Catalog Number
013111-000 FDA UDI
Primary DI / UDI-DI
D6860131119 FDA UDI
510(k) Number
K970594 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Alginate dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 FDA UDI
Commercial Distribution
Not 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

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

Dimensions & Sizes

Size
Weight — 1 Pound FDA UDI

Waterpik Key-To Alginate Impression Material by Water Pik, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Water Pik, Inc.

Sources (1)

  • FDA UDI 32c13680-bd80-4b60-a146-0e9e35b427f9 39 fields · synced Jun 8, 2026