HOHT LLC

FDA Device Registration & Listing · Danbury, CT, US · Registration 3042023934

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
3042023934
FEI Number
3042023934
Entity Name
HOHT LLC
City/State/Country
Danbury, CT, US
Establishment Address
83 Wooster Hts Ste 125, Danbury, CT 06810, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
HOHT LLC (Owner Number: 10094314)
Owner / Operator Contact Address
83 Wooster Heights, Ste 125, Danbury, CT 06810, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tube-Evac

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2025-11-23

Official Correspondent

Amanda Lowe

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

HOHT LLC
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 3042023934. Last updated year: 2026. Please use registration number 3042023934 when referencing this establishment in official correspondence.
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