← Back to catalogue

Jade

FDA UDI

Class II (US FDA UDI)

by Dharma Research, Inc.

Identity

Trade Name
Jade FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
Jade Green 37% Phosphoric Acid Etchant Gel - 4 x 1.2ml Syringes, 20 Pre-bent 23ga Tips & Instruction Insert FDA UDI
Model / Reference
20-00008 FDA UDI
Description
Jade Green 37% Phosphoric Acid Etchant Gel - 4 x 1.2ml Syringes, 20 Pre-bent 23ga Tips & Instruction Insert FDA UDI

Identifiers

Catalog Number
20-00008 FDA UDI
Primary DI / UDI-DI
00353045000697 FDA UDI
510(k) Number
K150696 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dental etching solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 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

Yes

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

Dimensions & Sizes

Size
Total Volume — 1.2 Milliliter FDA UDI

Category: Dental etching solution

Jade by Dharma Research, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental etching solution.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a3c6e194-bfe4-434d-ad34-1c7a51c3057f 38 fields · synced Jun 6, 2026