MEDICAL MONOFILAMENT MANUFACTURING

FDA Device Registration & Listing · Plymouth, MA, US · Registration 1226347

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
1226347
FEI Number
3002957596
Entity Name
MEDICAL MONOFILAMENT MANUFACTURING
City/State/Country
Plymouth, MA, US
Establishment Address
121 Camelot Dr Ste 2, Plymouth, MA 02360, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MEDICAL MONOFILAMENT MANUFACTURING (Owner Number: 9040501)
Owner / Operator Contact Address
Medical Monofilament, 121 Camelot Dr. Unit 2, Plymouth, MA 02360, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Fit2Walk Monofilament Sensory Screening Tool Monofilament Sensory Screening Tool SENSORY TESTIN NYLON FILAMENT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GXB Esthesiometer Neurology Class 1 882.1500 2015-02-04
GXB Esthesiometer Neurology Class 1 882.1500 2000-02-24

Official Correspondent

Michelle Hardiman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MEDICAL MONOFILAMENT MANUFACTURING
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1226347. Last updated year: 2026. Please use registration number 1226347 when referencing this establishment in official correspondence.
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