← 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
Screw endosteal dental implant, one-piece FDA UDI
Device Name
* UNIV STD ABUT HX 5HD 5.5CW 5.5CH W/SCREW #19503012 (TI6AL4VELI) FDA UDI
Model / Reference
01404512 FDA UDI
Description
* UNIV STD ABUT HX 5HD 5.5CW 5.5CH W/SCREW #19503012 (TI6AL4VELI) FDA UDI

Identifiers

Catalog Number
01404512 FDA UDI
Primary DI / UDI-DI
00614950000876 FDA UDI
510(k) Number
K954513 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Screw endosteal dental implant, one-piece 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

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Dimensions & Sizes

Size
Width — 5.5 Millimeter FDA UDI

Category: Screw endosteal dental implant, one-piece

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

Similar devices

Also classified as Screw endosteal dental implant, one-piece.

Cleared under the same submission

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 07862902-d104-430f-a9f1-59abaed2eac7 37 fields · synced May 30, 2026