Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Andover Healthcare Inc.

United States·US-MF-000035055

Last updated September 18, 2026

About

WELCOME TO OVIK HEALTH Advanced Clinical Products that advance your Care We’re your partners in problem solving. From advanced wound care to antimicrobial silver and Active Fluid Management®, our products and technologies are designed to take care further. Get to Know OVIK Health We are a team of innovators, advancing healthcare technologies to improve patient \[…\]

From the manufacturer's own website. Source

Information

Country
United States
Address
9, Fanaras Drive, Salisbury, MA, United States
LinkedIn
—
Facebook
—
Phone
+1 864 237 1520
PRRC Contact
Sherry Albritton
EUDAMED SRN
US-MF-000035055
FDA FEI Number
—
DUNS Number
088528245

Catalogue (122)

Page 1 of 3
DeviceModel / ReferenceRegistriesClassStatus
AndoFlex NL ASP-5400L-018
EUDAMED
Class IActive
Powerflex 6yd 3710WH-048
EUDAMED
Class IActive
Powerflex 6yd 3730BL-016
EUDAMED
Class IActive
Powerflex 6yd 4730BK-048
EUDAMED
Class IActive
PowerFlex Latex Free 4830WH-016
EUDAMED
Class IActive
Powerflex 6yd 3730GY-016
EUDAMED
Class IActive
Powerflex 6yd 3720PU-024
EUDAMED
Class IActive
AndoFlex TLC Zinc Standard ASP-8840UBZ-SC
EUDAMED
Class IActive
Powerflex 6yd 3720LB-024
EUDAMED
Class IActive
Powerflex 6yd 3720OR-024
EUDAMED
Class IActive
Powerflex 6yd 3730PU-016
EUDAMED
Class IActive
Powerflex 6yd 3725BK-016
EUDAMED
Class IActive
Powerflex 6yd 3720YL-024
EUDAMED
Class IActive
Powerflex 6yd 3730NV-016
EUDAMED
Class IActive
PowerFlex 5yard 3815WH-048
EUDAMED
Class IActive
Powerflex 6yd 4725WH-048
EUDAMED
Class IActive
Powerflex 6yd 3730MR-016
EUDAMED
Class IActive
Powerflex 6yd 3720NV-024
EUDAMED
Class IActive
Powerflex 6yd 3715NV-032
EUDAMED
Class IActive
Powerflex 6yd 3720BL-024
EUDAMED
Class IActive
Umafd 9430UM-01
EUDAMED
Class IActive
Powerflex 6yd 4725BK-048
EUDAMED
Class IActive
Powerflex 6yd 3720NP-024
EUDAMED
Class IActive
Powerflex 6yd 4730WH-048
EUDAMED
Class IActive
Powerflex 6yd 3710NV-048
EUDAMED
Class IActive
Powerflex 6yd 3720MR-024
EUDAMED
Class IActive
PowerFlex Latex Free 4815WH-032
EUDAMED
Class IActive
Powerflex 6yd 3760WH-08
EUDAMED
Class IActive
Powerflex 6yd 3730RD-016
EUDAMED
Class IActive
Powerflex 6yd 3715BL-032
EUDAMED
Class IActive
Powerflex 6yd 3760BK-08
EUDAMED
Class IActive
Powerflex 6yd 3715RD-032
EUDAMED
Class IActive
Powerflex 6yd 3715BK-032
EUDAMED
Class IActive
Powerflex 6yd 3720GY-024
EUDAMED
Class IActive
PowerFlex Latex Free 4820WH-024
EUDAMED
Class IActive
AndoFlex TLC Calamine Standard ASP-8840UBC-SC
EUDAMED
Class IActive
Powerflex 6yd 3720WH-024
EUDAMED
Class IActive
PowerFlex 5yard 3815RD-048
EUDAMED
Class IActive
CoFlex TLC Calamine Standard 8830UBC-SC-INTL
EUDAMED
Class IActive
Powerflex 6yd 3730OR-016
EUDAMED
Class IActive
Coflex Med 7150TN-048
EUDAMED
Class IActive
AndoFlex NL ASP-5400TN-018
EUDAMED
Class IActive
Powerflex 6yd 3720GR-024
EUDAMED
Class IActive
Powerflex 6yd 3730GR-016
EUDAMED
Class IActive
Powerflex 6yd 3720TN-024
EUDAMED
Class IActive
AndoFlex TLC Calamine Standard ASP-8830UBC-SC
EUDAMED
Class IActive
Powerflex 6yd 3720RD-024
EUDAMED
Class IActive
AndoFlex TLC Zinc Standard ASP-8830UBZ-SC
EUDAMED
Class IActive
AndoFlex TLC Calamine Lite ASP-8840UBC-TN
EUDAMED
Class IActive
Powerflex 6yd 3715WH-032
EUDAMED
Class IActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (7)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Apr 2, 2024Z-1828-2024—open, classified

A packaging seal gap could impact the sterility of the product.

Jun 19, 2019Z-0179-2020—terminated

Incomplete packaging seal of sterile product

Jun 19, 2019Z-0181-2020—terminated

Incomplete packaging seal of sterile product

Jun 19, 2019Z-0183-2020—terminated

Incomplete packaging seal of sterile product

Jun 19, 2019Z-0184-2020—terminated

Incomplete packaging seal of sterile product

Jun 19, 2019Z-0180-2020—terminated

Incomplete packaging seal of sterile product

Jun 19, 2019Z-0182-2020—terminated

Incomplete packaging seal of sterile product