Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1220799

FEI Number

1220799

Entity Name

ANDOVER HEALTHCARE, INC.

City/State/Country

SALISBURY, MA, US

Establishment Address

9 Fanaras Dr, SALISBURY, MA 01952, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ANDOVER HEALTHCARE, INC. (Owner Number: 1220799)

Owner / Operator Contact Address

9 FANARAS DR., --, Salisbury, MA 01952, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Care Kit Calamine Care Kit Zn CoFlex TLC, Two Layer Compression Moleskin, Cloth Medical Tape CoFlex UBC, CoFlex UBZ

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ITG	Bandage, Cast	Physical Medicine	Class 1	890.3025	2017-02-01
MHW	Dressing, Compression	General Hospital	Class 1	880.5075	2020-12-20
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	1992-08-10

Official Correspondent

Sherry Albritton

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ANDOVER HEALTHCARE, INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29
K870091	Avery Intl.	IV SECUREMENT DEVICE USING PCCE THERMO. FILM	1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1220799. Last updated year: 2026. Please use registration number 1220799 when referencing this establishment in official correspondence.