← Back to catalogue

Insole D-Sole 1/4in Thick

FDA UDI

Class I (US FDA UDI)

by AliMed, LLC

Identity

Trade Name
INSOLE D-SOLE 1/4IN THICK FDA UDI
Generic Name
Foot orthosis FDA UDI
Model / Reference
6227/NA/D FDA UDI

Identifiers

Catalog Number
2970004074 FDA UDI
Primary DI / UDI-DI
00733657247381 FDA UDI
FDA Product Code
KYS FDA UDI
GMDN Term
Foot orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6280 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

Yes

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

Yes

FDA UDI

Category: Foot orthosis

Insole D-Sole 1/4in Thick by AliMed, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foot orthosis.

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
AliMed, LLC

Sources (1)

  • FDA UDI 272e2e37-e995-4b8d-a4db-98778eb3bfae 34 fields · synced Jun 9, 2026