PLYMOUTH MEDICAL

FDA Device Registration & Listing · Brooklyn, NY, US · Registration 3028002947

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
3028002947
FEI Number
3028002947
Entity Name
PLYMOUTH MEDICAL
City/State/Country
Brooklyn, NY, US
Establishment Address
135 Plymouth St # 310, Brooklyn, NY 11201, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Custom Compounding LLC dba PLYMOUTH MEDICAL (Owner Number: 10095251)
Owner / Operator Contact Address
135 Plymouth Street 310, Brooklyn, NY 11201, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
BK251196
PMA Number
N/A

All Registered Proprietary Names

Convenience Kit with ACD-A Exocube Aest Kit 60/ EXO60Kit-A Centrifuge Container Kit 120/ PRP120Kit Centrifuge Container Kit 60/ PRP60Kit ExoCube Kit 60/ EXO60Kit ExoCube Kit 120/ EXO120Kit Convenience Kit with ACD-A

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KDD Kit, Surgical Instrument, Disposable General, Plastic Surgery Class 1 878.4800 2026-04-07
ORG Platelet And Plasma Separator For Bone Graft Handling Hematology Class 2 864.9245 2026-02-16

Official Correspondent

Jo-An Tremblay

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Custom Compounding LLC dba PLYMOUTH MEDICAL
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 3028002947. Last updated year: 2026. Please use registration number 3028002947 when referencing this establishment in official correspondence.
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