← Back to catalogue

Ace

FDA UDI

Class II (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
ACE FDA UDI
Generic Name
Dental prosthesis/implant abutment screw analog, single-use FDA UDI
Device Name
CLOSED TRAY IMP COPING 4 & 5HD STD ABUT 5.5CW W/19522001 FDA UDI
Model / Reference
03604022 FDA UDI
Description
CLOSED TRAY IMP COPING 4 & 5HD STD ABUT 5.5CW W/19522001 FDA UDI

Identifiers

Catalog Number
03604022 FDA UDI
Primary DI / UDI-DI
00614950021505 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Dental prosthesis/implant abutment screw analog, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental prosthesis/implant abutment screw analog, single-use

Ace by Ace Surgical Supply Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental prosthesis/implant abutment screw analog, single-use.

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

Sources (1)

  • FDA UDI 29805d7c-faca-4469-b8c2-2bc3680d513d 36 fields · synced May 31, 2026