Air Flex with Auto-Distraction

FDA UDI

Class II (US FDA UDI)

by Hill Laboratories

Identity

Trade Name: Air Flex with Auto-Distraction FDA UDI
Generic Name: Body arch traction table FDA UDI
Model / Reference: Air Flex II with Auto-Distraction FDA UDI

Identifiers

Primary DI / UDI-DI: 00860001452525 FDA UDI
510(k) Number: K063034 FDA UDI
FDA Product Code: JFB FDA UDI
GMDN Term: Body arch traction table FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.5880 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Body arch traction table

Air Flex with Auto-Distraction by Hill Laboratories — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Body arch traction table.

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Hill Laboratories

Sources (1)

FDA UDI 65b9d0d7-672d-45bd-9935-5609c7e1dc20 33 fields · synced May 30, 2026