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Neck Extractor

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
Neck Extractor FDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Device Name
Neck Extractor FDA UDI
Model / Reference
Neck Extractor FDA UDI
Description
Neck Extractor FDA UDI

Identifiers

Catalog Number
9095.11.101 FDA UDI
Primary DI / UDI-DI
08033390085274 FDA UDI
510(k) Number
K141327 FDA UDI
FDA Product Code
MBL FDA UDI
LZO FDA UDI
JDI FDA UDI
KWY FDA UDI
KWZ FDA UDI
LPH FDA UDI
GMDN Term
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3353 FDA UDI
888.3350 FDA UDI
888.3390 FDA UDI
888.3310 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic inorganic implant inserter/extractor, reusable

Neck Extractor by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic inorganic implant inserter/extractor, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 2a8a17c5-9550-4e82-8673-2ab038766930 35 fields · synced May 30, 2026