← Back to catalogue

Micron

FDA UDI

Class II (US FDA UDI)

by Gyrus Acmi, Inc.

Identity

Trade Name
MICRON FDA UDI
Generic Name
Ossicular prosthesis, total FDA UDI
Device Name
MICRON II ALL TITANIUM CENTERED TORP 7.00MM TITANIUM TILT TOP HEAD FDA UDI
Model / Reference
70142016 FDA UDI
Description
MICRON II ALL TITANIUM CENTERED TORP 7.00MM TITANIUM TILT TOP HEAD FDA UDI

Identifiers

Primary DI / UDI-DI
00821925023512 FDA UDI
510(k) Number
K002737 FDA UDI
FDA Product Code
ETA FDA UDI
GMDN Term
Ossicular prosthesis, total FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3495 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ossicular prosthesis, total

Micron by Gyrus Acmi, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ossicular prosthesis, total.

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

Manufacturer
Gyrus Acmi, Inc.

Sources (1)

  • FDA UDI d569ba25-9b73-4428-ad6f-c17c6c032a8a 35 fields · synced Jun 8, 2026