Danzach Corp

FDA Device Registration & Listing · Pottstown, PA, US · Registration 3008017452

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
3008017452
FEI Number
3008017452
Entity Name
Danzach Corp
City/State/Country
Pottstown, PA, US
Establishment Address
321 JONES BLVD STE 112, Pottstown, PA 19464, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Danzach Corp (Owner Number: 10030789)
Owner / Operator Contact Address
321 Jones Blvd, Ste 112, Pottstown, PA 19464, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Spoon, ophthalmic SCISSORS, GENERAL, SURGICAL MIRROR, ENT Cannula and trocar, suprapubic, non-disposable

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HNB Spoon, Ophthalmic Ophthalmic Class 1 886.4350 2020-08-18
LRW Scissors, General, Surgical General, Plastic Surgery Class 1 878.4800 2016-01-29
KAI Mirror, Ent Ear, Nose, Throat Class 1 874.4420 2020-08-10
FBM Cannula And Trocar, Suprapubic, Non-Disposable Gastroenterology, Urology Class 1 876.5090 2022-01-19

Official Correspondent

Dan Cusack

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Danzach Corp
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 3008017452. Last updated year: 2026. Please use registration number 3008017452 when referencing this establishment in official correspondence.
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