Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003270419

FEI Number

3003270419

Entity Name

CASCO BAY MOLDING

City/State/Country

Sanford, ME, US

Establishment Address

32 Smada Dr, Sanford, ME 04073, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Casco Bay Molding (Owner Number: 10051516)

Owner / Operator Contact Address

32 Smada Drive, Sanford, ME 04073, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

August Cup Casco Cup Lincup by Lintimate myEverCup Aria Cup Best, Periodt. Cheremi Maka Casco Disc UltuCup Cherry Cup Wandah FemCap Chewy Tubes Tentacle Teether Back to Mom Nipple Shield Weaning Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HHE	Cup, Menstrual	Obstetrics/Gynecology	Class 2	884.5400	2016-03-29
HGD	Applicator, Vaginal	Obstetrics/Gynecology	Class 1	884.4520	2026-05-29
LLQ	Cap, Cervical, Contraceptive	Unknown	Class 3	N/A	2026-01-27
MEF	Ring, Teething, Non-Fluid Filled	Dental	Class 1	872.5550	2022-01-26
HFS	Shield, Nipple	General Hospital	Class 1	880.5630	2020-12-17

Official Correspondent

Andrew Powell

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Casco Bay Molding

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 3003270419. Last updated year: 2026. Please use registration number 3003270419 when referencing this establishment in official correspondence.