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ACE Surgical

FDA UDI

Class I (US FDA UDI)

by Prismatik Dentalcraft, Inc.

Identity

Trade Name
ACE Surgical FDA UDI
Generic Name
Dental implant analog FDA UDI
Device Name
ACE Surgical TRI-CAM Implant Analog for 6.0 mm FDA UDI
Model / Reference
307606 FDA UDI
Description
ACE Surgical TRI-CAM Implant Analog for 6.0 mm FDA UDI

Identifiers

Catalog Number
307606 FDA UDI
Primary DI / UDI-DI
D7453076060 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant analog FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

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

Yes

FDA UDI

Dimensions & Sizes

Size
Height — 11 Millimeter FDA UDI

Category: Dental implant analog

ACE Surgical by Prismatik Dentalcraft, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant analog.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 452a9e7d-0104-49ce-92f6-24f566e1ff6b 36 fields · synced May 29, 2026