SOLSTICE CORPORATION

FDA Device Registration & Listing · South Portland, ME, US · Registration 1221946

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
1221946
FEI Number
1221946
Entity Name
SOLSTICE CORPORATION
City/State/Country
South Portland, ME, US
Establishment Address
190 Sawyer Street, South Portland, ME 04106, US
Establishment Type(s)
Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
SOLSTICE CORPORATION (Owner Number: 1221946)
Owner / Operator Contact Address
190 Sawyer Street, South Portland, ME 04106, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

VARIOUS SIZE NON-STERILE A

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KXF Applicator, Absorbent Tipped, Non-Sterile General Hospital Class 1 880.6025 1992-08-06

Official Correspondent

DANFORTH DESENA

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SOLSTICE CORPORATION
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 1221946. Last updated year: 2026. Please use registration number 1221946 when referencing this establishment in official correspondence.
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