C2C DEVELOPMENT, LLC

FDA Device Registration & Listing · Melbourne, FL, US · Registration 3011193444

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
3011193444
FEI Number
3011193444
Entity Name
C2C DEVELOPMENT, LLC
City/State/Country
Melbourne, FL, US
Establishment Address
1135 W NASA Blvd Suite 102, Melbourne, FL 32901, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
C2C Development, LLC (Owner Number: 10047566)
Owner / Operator Contact Address
1135 W Nasa Blvd, Suite 500, Melbourne, FL 32901, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

GENOSYL DS Mixer Pain Precision Cannula Kit Pain Flow Nerve Block Pain Control Nerve Block Gas Inlet Adapter GENOSYL DS Vapotherm Accessory Kit GENOSYL DS HFOV Gas Sampling Port GENOSYL DS Manual Ventilation Bag NO Adapter GENOSYL DS Bunnell Adapter GENOSYL DS Sample Line Extension GENOSYL DS Bunnell Tee Adapters Adaptive Sensor Gas Line Set

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MRN Apparatus, Nitric Oxide Delivery Anesthesiology Class 2 868.5165 2020-04-14
OIL Discography Kit Radiology Class 2 892.1730 2024-01-19
CAZ Anesthesia Conduction Kit Anesthesiology Class 2 868.5140 2024-01-19
BZO Set, Tubing And Support, Ventilator (W Harness) Anesthesiology Class 1 868.5975 2020-04-09

Official Correspondent

Craig Pagan

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

C2C Development, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0028-2026 NOXBOX LTD 2
NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I
Z-0029-2026 NOXBOX LTD 2
NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I
Z-0031-2026 Percussionaire Corporation 1
Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011193444. Last updated year: 2026. Please use registration number 3011193444 when referencing this establishment in official correspondence.
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