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Wave

FDA UDI

Class II (US FDA UDI)

by Sdi , Ltd.

Identity

Trade Name
WAVE FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
WAVE 1 SYR A1 FDA UDI
Model / Reference
7510102 FDA UDI
Description
WAVE 1 SYR A1 FDA UDI

Identifiers

Catalog Number
7510102 FDA UDI
Primary DI / UDI-DI
09336472008475 FDA UDI
510(k) Number
K973091 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental composite resin

Wave by Sdi , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sdi , Ltd.

Sources (1)

  • FDA UDI f5f8a2b8-438c-4ad7-a3d9-8b8f8f6bb923 36 fields · synced May 30, 2026