Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

DeVilbiss Healthcare LLC.

US

Last updated September 17, 2026

Information

Country
US
Address
100 Devilbiss Dr, SOMERSET, PA, 15501
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
2515872
DUNS Number
—

Catalogue (314)

Page 2 of 7
DeviceModel / ReferenceRegistriesClassStatus
DeVilbiss 3655I
FDA UDI
Class IIUnknown
DeVilbiss 119
FDA UDI
Class IUnknown
DeVilbiss 535C-M6-CF
FDA UDI
Class IIUnknown
DeVilbiss DV54D-LA
FDA UDI
Class IIUnknown
DeVilbiss 7305P-G
FDA UDI
Class IIUnknown
DeVilbiss DV51D-HH-S-HT
FDA UDI
Class IIUnknown
DeVilbiss 180
FDA UDI
Class IIUnknown
DeVilbiss DV54NE-P
FDA UDI
Class IIUnknown
DeVilbiss PD1000I
FDA UDI
Class IIUnknown
DeVilbiss 3655A
FDA UDI
Class IIUnknown
DeVilbiss 3655PL-AMSS
FDA UDI
Class IIUnknown
DeVilbiss 535D-C-CF
FDA UDI
Class IIActive
DeVilbiss 3655PL-WW
FDA UDI
Class IIUnknown
DeVilbiss DV53D-R
FDA UDI
Class IIUnknown
DeVilbiss PD1000A-M6
FDA UDI
Class IIUnknown
DeVilbiss 7305D-LA
FDA UDI
Class IIUnknown
DeVilbiss DV51UK-HH
FDA UDI
Class IIUnknown
DeVilbiss PD1000A-I-C
FDA UDI
Class IIUnknown
DeVilbiss DV53D
FDA UDI
Class IIUnknown
DeVilbiss 15-RD
FDA UDI
Class IUnknown
DeVilbiss DV56D
FDA UDI
Class IIUnknown
DeVilbiss 7314P-NE
FDA UDI
Class IIUnknown
DeVilbiss DV56NE
FDA UDI
Class IIUnknown
DeVilbiss 7314P-AP
FDA UDI
Class IIUnknown
DeVilbiss 8650D
FDA UDI
Class IIUnknown
DeVilbiss 535C-C-870
FDA UDI
Class IIUnknown
DeVilbiss DV56BR-HH
FDA UDI
Class IIUnknown
DeVilbiss 535C-C-CF
FDA UDI
Class IIUnknown
DeVilbiss 6910D-DR
FDA UDI
Class IIActive
DeVilbiss 3655PL-PHYS
FDA UDI
Class IIUnknown
DeVilbiss 3655PL-S4H
FDA UDI
Class IIUnknown
DeVilbiss 535D-E-870
FDA UDI
Class IIUnknown
DeVilbiss PD1000A-CAN-C
FDA UDI
Class IIUnknown
DeVilbiss DV55NE
FDA UDI
Class IIUnknown
DeVilbiss 535I-E-CF
FDA UDI
Class IIUnknown
DeVilbiss DV51D-HH-S
FDA UDI
Class IIUnknown
DeVilbiss DV57D-HH-S2
FDA UDI
Class IIUnknown
DeVilbiss DV55D
FDA UDI
Class IIUnknown
DeVilbiss 535C-D-CF
FDA UDI
Class IIUnknown
DeVilbiss 175
FDA UDI
Class IUnknown
DeVilbiss DV56NE-HH
FDA UDI
Class IIUnknown
DeVilbiss 177
FDA UDI
Class IActive
DeVilbiss DV51D-HH-HT
FDA UDI
Class IIUnknown
DeVilbiss 7310PD-S
FDA UDI
Class IIUnknown
DeVilbiss DV56D-HH-S
FDA UDI
Class IIUnknown
DeVilbiss 5650P
FDA UDI
Class IIUnknown
DeVilbiss DV57D-LA
FDA UDI
Class IIUnknown
DeVilbiss 7305P-T
FDA UDI
Class IIUnknown
DeVilbiss 5650C
FDA UDI
Class IIUnknown
DeVilbiss 3655LTPL-KMP
FDA UDI
Class IIUnknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (6)

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
Mar 9, 2023Z-1558-2023—open, classified

The instruction manual is being replaced with an updated version that is in alignment with labeling requirements specified in the IEC-60101-1 standard.

Nov 18, 2022Z-0724-2023—open, classified

The firm has received complaints of the device becoming hot. The firm has updated the user manual to include warnings that applied parts in contact with the patient may in some situations exceed 41 degrees Celsius (105.8 degrees Fahrenheit), clarification on expected service life, and the need for maintenance to certain components.

Sep 19, 2022Z-0229-2023—open, classified

An unapproved adhesive used to manufacture the accumulator tank sub assembly (a part of the patient gas pathway)

May 23, 2016Z-2246-2016—terminated

A small percentage of units of 7305 Series Vacu-Aide Suction Units are experiencing premature failure during operation.

May 13, 2014Z-1949-2014—terminated

A limited number of DV5x Series CPAP units were manufactured and shipped without the serial number programmed into the unit, causing the unit serial number on LCD display to appear as "RUN-TEST".

Mar 7, 2013Z-2319-2013—terminated

End users of the DeVilbiss Disposable Suction Container/Filter had exposed the bacterial filter cartridge to fluid, thereby occluding the filter and rendering it unusable.