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Cure Lp

FDA UDI

Class II (US FDA UDI)

by Meditech Spine, Llc

Identity

Trade Name
CURE LP FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Model / Reference
900-909-13 FDA UDI

Identifiers

Primary DI / UDI-DI
B167900909130 FDA UDI
510(k) Number
K171538 FDA UDI
FDA Product Code
KWQ FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Cure Lp by Meditech Spine, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Meditech Spine, Llc

Sources (1)

  • FDA UDI 3b21ccac-0896-4a4b-a9a6-22ea368a688e 33 fields · synced May 31, 2026