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F8x Lacer Ankle W/Stays Lg

FDA UDI

Class I (US FDA UDI)

by Bird & Cronin, Llc

Identity

Trade Name
F8X LACER ANKLE W/STAYS LG FDA UDI
Generic Name
Ankle/foot orthosis FDA UDI
Model / Reference
90007758 FDA UDI

Identifiers

Primary DI / UDI-DI
00610570184231 FDA UDI
FDA Product Code
ITW 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ankle/foot orthosis

F8x Lacer Ankle W/Stays Lg by Bird & Cronin, 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
Bird & Cronin, Llc

Sources (1)

  • FDA UDI 82a08440-9413-4afb-bba3-388b13ef2159 32 fields · synced May 30, 2026