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Henry Schein

FDA UDI

Class II (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name
Henry Schein FDA UDI
Generic Name
Cryogenic spray, dental FDA UDI
Device Name
Endo Cool Spray FDA UDI
Model / Reference
1125056 FDA UDI
Description
Endo Cool Spray FDA UDI

Identifiers

Catalog Number
1125056 FDA UDI
Primary DI / UDI-DI
H65811250560 FDA UDI
510(k) Number
K930764 FDA UDI
FDA Product Code
EAT FDA UDI
GMDN Term
Cryogenic spray, dental FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1720 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

No

FDA UDI

Category: Cryogenic spray, dental

Henry Schein by Henry Schein, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cryogenic spray, dental.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Henry Schein, Inc.

Sources (1)

  • FDA UDI fd52e987-f60c-4a8b-abea-474cf224a577 36 fields · synced May 30, 2026