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Avalign

FDA UDI

Class I (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name
Avalign FDA UDI
Generic Name
Middle ear pick FDA UDI
Device Name
Pick, medium, angled, FDA UDI
Model / Reference
VM101-4444 FDA UDI
Description
Pick, medium, angled, FDA UDI

Identifiers

Primary DI / UDI-DI
00190776044183 FDA UDI
FDA Product Code
JYT FDA UDI
GMDN Term
Middle ear pick FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

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: Middle ear pick

Avalign is a high-quality, reusable fine-handheld surgical instrument designed to facilitate precise and effective middle ear procedures. Specifically, it's an angled pick used for delicate tasks in microsurgical ear surgery.

Similar devices

Also classified as Middle ear pick.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AVALIGN TECHNOLOGIES, Inc.

Sources (1)

  • FDA UDI 989abfd1-caa2-4a60-84de-43748785ad78 34 fields · synced Jul 17, 2026