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Implant Spacers

FDA UDI

Class I (US FDA UDI)

by Suncoast Dental, Inc.

Identity

Trade Name
Implant Spacers FDA UDI
Generic Name
Dental implantation depth/angle gauge, reusable FDA UDI
Device Name
Implant Spacers Set#1- for approximating space between teeth and/or implants - 1.5, 2.0, 2.5, 3.0, 3.5, & 4.0mm FDA UDI
Model / Reference
Implant Spacers Set#1 FDA UDI
Description
Implant Spacers Set#1- for approximating space between teeth and/or implants - 1.5, 2.0, 2.5, 3.0, 3.5, & 4.0mm FDA UDI

Identifiers

Catalog Number
Implant Spacers Set #1 FDA UDI
Primary DI / UDI-DI
00083208190018 FDA UDI
FDA Product Code
KMY FDA UDI
GMDN Term
Dental implantation depth/angle gauge, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5525 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implantation depth/angle gauge, reusable

Implant Spacers by Suncoast Dental, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implantation depth/angle gauge, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 90d44582-d2c1-490c-9fe8-7852ef3ddb7d 35 fields · synced Jun 7, 2026