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Donjoy Performance

FDA UDI

Class I (US FDA UDI)

by Djo, Llc

Identity

Trade Name
DONJOY PERFORMANCE FDA UDI
Generic Name
Ankle/foot orthosis FDA UDI
Device Name
POD ANKLE, White, X-Small, Right FDA UDI
Model / Reference
DP151AB05-WHT-XS-R FDA UDI
Description
POD ANKLE, White, X-Small, Right FDA UDI

Identifiers

Primary DI / UDI-DI
00888912162630 FDA UDI
FDA Product Code
IQI FDA UDI
GMDN Term
Ankle/foot orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ankle/foot orthosis

Donjoy Performance by Djo, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ankle/foot orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI 04885150-e9d1-4114-a50a-d990a37702a2 33 fields · synced May 30, 2026