← Back to catalogue

Sealing Cap (Size 9)

FDA UDI

Class II (US FDA UDI)

by Sonendo, Inc.

Identity

Trade Name
Sealing Cap (Size 9) FDA UDI
Generic Name
Dental delivery system instrument unit, electric FDA UDI
Device Name
Sealing Caps attach to the Molar Procedure Instrument in order to properly setup the Procedure Instrument for teeth of different pulp chamber depths. The Sealing Caps include a color-coded surface to match the proper Sealing Cap to the proper Depth Gauge. Additionally, Sealing Caps feature a sealing element intended to keep air out of the root canal system and procedure fluid inside the tooth. FDA UDI
Model / Reference
FG-001-00009 FDA UDI
Description
Sealing Caps attach to the Molar Procedure Instrument in order to properly setup the Procedure Instrument for teeth of different pulp chamber depths. The Sealing Caps include a color-coded surface to match the proper Sealing Cap to the proper Depth Gauge. Additionally, Sealing Caps feature a sealing element intended to keep air out of the root canal system and procedure fluid inside the tooth. FDA UDI

Identifiers

Catalog Number
GW-MOL-SP09 FDA UDI
Primary DI / UDI-DI
00858395006073 FDA UDI
FDA Product Code
ELC FDA UDI
GMDN Term
Dental delivery system instrument unit, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Category: Dental delivery system instrument unit, electric

Sealing Cap (Size 9) by Sonendo, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental delivery system instrument unit, electric.

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

Manufacturer
Sonendo, Inc.

Sources (1)

  • FDA UDI 2ddc8375-c29d-4370-99b9-25e9e0c4a481 36 fields · synced Jun 6, 2026