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Trulife

FDA UDI

Class I (US FDA UDI)

by Trulife, Inc.

Identity

Trade Name
Trulife FDA UDI
Generic Name
Mechanical-resistance external ankle-foot prosthesis FDA UDI
Device Name
TRULIFE ZENITH FOOT 24CM LEFT CAT 1 DK BRN FDA UDI
Model / Reference
SZN203-24-L-1 FDA UDI
Description
TRULIFE ZENITH FOOT 24CM LEFT CAT 1 DK BRN FDA UDI

Identifiers

Primary DI / UDI-DI
00645517872162 FDA UDI
FDA Product Code
ISH FDA UDI
GMDN Term
Mechanical-resistance external ankle-foot prosthesis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Mechanical-resistance external ankle-foot prosthesis

Trulife by Trulife, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mechanical-resistance external ankle-foot prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Trulife, Inc.

Sources (1)

  • FDA UDI d63ea85a-abb6-4296-bd77-0dde6c1581c5 33 fields · synced Jun 4, 2026