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Ankylos®

FDA UDI

Class I (US FDA UDI)

by Dentsply Implants Manufacturing GmbH

Identity

Trade Name
ANKYLOS® FDA UDI
Generic Name
Surgical instrument/endoscope cleaning utensil, reusable FDA UDI
Device Name
Drill Cleaning Instrument FDA UDI
Model / Reference
31037320 FDA UDI
Description
Drill Cleaning Instrument FDA UDI

Identifiers

Catalog Number
31037320 FDA UDI
Primary DI / UDI-DI
07392532220258 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Surgical instrument/endoscope cleaning utensil, reusable 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

No

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

No

FDA UDI

Category: Surgical instrument/endoscope cleaning utensil, reusable

Ankylos® by Dentsply Implants Manufacturing GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument/endoscope cleaning utensil, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f7ca6803-9b74-4430-acab-5a7cb01a7c2a 34 fields · synced May 30, 2026