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Ace

FDA UDI

Class I (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
ACE FDA UDI
Generic Name
Dental osteotome FDA UDI
Device Name
SINUS LIFT OSTEOTOME 1.6/2MM 6"/15CM (SS 17-4 1-1900) FDA UDI
Model / Reference
4545001 FDA UDI
Description
SINUS LIFT OSTEOTOME 1.6/2MM 6"/15CM (SS 17-4 1-1900) FDA UDI

Identifiers

Catalog Number
4545001 FDA UDI
Primary DI / UDI-DI
00614950030910 FDA UDI
FDA Product Code
EMM FDA UDI
GMDN Term
Dental osteotome FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental osteotome

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

Similar devices

Also classified as Dental osteotome.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 072b99ab-2e0c-4caa-b692-e56efa2e06c1 35 fields · synced Jun 8, 2026