NEW WAVE ENDO

FDA Device Registration & Listing · Coconut Creek, FL, US · Registration 3015209038

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015209038
FEI Number
3015209038
Entity Name
NEW WAVE ENDO
City/State/Country
Coconut Creek, FL, US
Establishment Address
6601 Lyons Road, Unit D8, Coconut Creek, FL 33073, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
New Wave Endo (Owner Number: 10060773)
Owner / Operator Contact Address
6601 Lyons Road, Unit D8, Coconut Creek, FL 33073, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

MPS Acacia Nerve Block Needle Nerve Block Needle

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAB Needle, Suturing, Disposable General, Plastic Surgery Class 1 878.4800 2024-03-11
CAZ Anesthesia Conduction Kit Anesthesiology Class 2 868.5140 2019-07-17

Official Correspondent

Martin Singer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

New Wave Endo
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015209038. Last updated year: 2026. Please use registration number 3015209038 when referencing this establishment in official correspondence.
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