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TRI-CAM Dental Implant System

FDA UDI

Class I (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
TRI-CAM Dental Implant System FDA UDI
Generic Name
Surgical drill guide, reusable FDA UDI
Device Name
TRI-CAM Drill 4.0mm x 16mm TL 4 Flutes Tapered FDA UDI
Model / Reference
30953005 FDA UDI
Description
TRI-CAM Drill 4.0mm x 16mm TL 4 Flutes Tapered FDA UDI

Identifiers

Catalog Number
30953005 FDA UDI
Primary DI / UDI-DI
00614950028276 FDA UDI
FDA Product Code
DZA FDA UDI
GMDN Term
Surgical drill guide, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 16 Millimeter FDA UDI

Category: Surgical drill guide, reusable

TRI-CAM Dental Implant System by Ace Surgical Supply Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drill guide, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 255d5360-e06a-4a4b-b3fa-3fca1b377d52 36 fields · synced May 31, 2026