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Ventlab Corp.

United States·US-MF-000008625

Last updated May 23, 2026

What Ventlab Corp. makes

Ventlab Corp. manufactures single-use manual pulmonary resuscitators, anaesthesia face masks, and anaesthesia breathing circuits. The company also produces non-ventilatory atomizers, non-powered airway pressure monitors, exhaled-gas oesophageal intubation detectors, single-use microbial medical gas filters, and basic nasal oxygen cannulas.

The company is based in the United States, and its portfolio consists of Class I and Class II medical devices. These products are listed within the FDA UDI database.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

Where is Ventlab Corp. based?

Ventlab Corp. is based in the United States. This location is confirmed by the company's official regulatory profile, which identifies the US as its primary base of operations.

What types of medical devices does Ventlab Corp. manufacture?

Ventlab Corp. manufactures a range of respiratory and anaesthesia equipment. Their product portfolio includes manual pulmonary resuscitators, anaesthesia face masks, anaesthesia breathing circuits, non-ventilatory atomizers, non-powered airway pressure monitors, exhaled-gas oesophageal intubation detectors, microbial medical gas filters, and basic nasal oxygen cannulas.

How are the devices from Ventlab Corp. classified?

The medical devices produced by Ventlab Corp. are classified as Class I and Class II. These classifications are based on the regulatory framework applied to the specific types of respiratory and anaesthesia equipment the company manufactures.

Which registries list the devices produced by Ventlab Corp.?

The devices manufactured by Ventlab Corp. are listed in the FDA UDI database. This registry is the official source for identifying the company's medical devices as required by regulatory standards.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: United States
Address: 2710 Northridge Dr. NW, Suite A, Grand Rapids, United States
Website: myairlife.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1-269-873-0502
PRRC Contact: Robert Yamashita
EUDAMED SRN: US-MF-000008625
FDA FEI Number: —
DUNS Number: —

Catalogue (1040)

Page 2 of 21

Device	Model / Reference	Registries	Class	Status
Ventlab	VN3100MB-B	FDA UDI	Class II	Active
Ventlab	SS3200MC	FDA UDI	Class II	Active
Ventlab	VN3100MB-D1	FDA UDI	Class II	Active
Ventlab	BT2027	FDA UDI	Class I	Active
Ventlab	HS1020	FDA UDI	Class II	Active
Ventlab	AF3140MC	FDA UDI	Class II	Active
Ventlab	VR0400-20	FDA UDI	Class I	Active
Ventlab	HS4051-B	FDA UDI	Class II	Unknown
Ventlab	VT3000	FDA UDI	Class II	Active
Ventlab	AF3040MB	FDA UDI	Class II	Active
Ventlab	VR0040-100	FDA UDI	Class I	Active
Ventlab	AF2002MB	FDA UDI	Class II	Active
Ventlab	5107GS-E	FDA UDI	Class II	Active
Ventlab	4307	FDA UDI	Class II	Active
Ventlab	HM10	FDA UDI	Class II	Active
Ventlab	VN2002MCP	FDA UDI	Class II	Active
Ventlab	AF2140MB-I	FDA UDI	Class II	Active
Ventlab	301-062213G	FDA UDI	Class II	Active
Ventlab	VN3100MBMO-D1	FDA UDI	Class II	Active
Ventlab	BR205	FDA UDI	Class II	Active
Ventlab	VR2900-20	FDA UDI	Class I	Active
Ventlab	AF5040MBP-E	FDA UDI	Class II	Active
Ventlab	VN2000MB-D3	FDA UDI	Class II	Active
Ventlanb	AF2142MB-2	FDA UDI	Class II	Active
Ventlab	HS4051-M0	FDA UDI	Class II	Unknown
Ventlab	AF5100MB	FDA UDI	Class II	Active
Ventlab	VN3100MB-I	FDA UDI	Class II	Active
Ventlab	PRO-6054	FDA UDI	Class II	Active
Ventlab	CS9006	FDA UDI	Class II	Active
Ventlab	AF1040MBS	FDA UDI	Class II	Active
Ventlab	AFD5140MB-T	FDA UDI	Class II	Active
Ventlab	2002HZ	FDA UDI	Class II	Active
Ventlab	BT4019	FDA UDI	Class I	Active
Ventlab	BT2215	FDA UDI	Class I	Active
Ventlab	BT5007F	FDA UDI	Class I	Active
Ventlab	3025G	FDA UDI	Class I	Unknown
Ventlab	AF1140MBP-M5	FDA UDI	Class II	Active
Ventlab	5107F-SE-E	FDA UDI	Class II	Active
Ventlab	AF3140MB-D12I	FDA UDI	Class II	Active
Ventlab	VN2100MX	FDA UDI	Class II	Active
Ventlab	AF3100MBP	FDA UDI	Class II	Active
Ventlab	HS34050-MMC	FDA UDI	Class II	Unknown
Ventlab	VT1000	FDA UDI	Class II	Active
Ventlab	VN3100MXK-2	FDA UDI	Class II	Active
Ventlab	AF5000MB-I	FDA UDI	Class II	Active
Ventlab	2003HZ	FDA UDI	Class II	Active
Ventlab	HM05	FDA UDI	Class II	Active
Ventlab	1100HF	FDA UDI	Class I	Active
Ventlab	VN5000MBPF	FDA UDI	Class II	Active
Ventlab	AF1000MB-PWTS5	FDA UDI	Class II	Unknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

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Authorities

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FDA Recalls (21)

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

Ventlab Corp. has 21 recall records initiated between April 15, 2003, and March 15, 2016, all of which are currently in terminated status. The reasons cited for these recalls include issues with pop-off valve functionality, potential separation of the breathing bag from the bushing, non-functional CO2 indicators, missing instructions regarding manometer verification, device cracking, and potential volume leakage through the inlet valve.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Mar 15, 2016	Z-1880-2016	—	terminated	Stat-check CO2 indicators are non-functional. The indicator is yellow when not in use and should be purple when not in use. The yellow indicates a 5% CO2 level, cardiac massage and ventiliation being performed correctly. The color will not change during use and will not be an indicator of CO2 level or improper performance of cardiac message and ventilation.
May 16, 2014	Z-1948-2014	—	terminated	The pop-off valve in the defective devices remain open and a squeeze of the bag may not generate enough force to force the duck bill valve open and therefore no air will be delivered to the victim.
Jul 11, 2012	Z-0177-2013	—	terminated	Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Jul 11, 2012	Z-0172-2013	—	terminated	Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Jul 11, 2012	Z-0176-2013	—	terminated	Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Jul 11, 2012	Z-0179-2013	—	terminated	Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Jul 11, 2012	Z-0174-2013	—	terminated	Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Jul 11, 2012	Z-0180-2013	—	terminated	Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Jul 11, 2012	Z-0175-2013	—	terminated	Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Jul 11, 2012	Z-0170-2013	—	terminated	Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Jul 11, 2012	Z-0173-2013	—	terminated	Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Jul 11, 2012	Z-0181-2013	—	terminated	Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Jul 11, 2012	Z-0171-2013	—	terminated	Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Jul 11, 2012	Z-0178-2013	—	terminated	Possible volume leakage through the inlet valve during compressions of the resuscitator bag.
Dec 5, 2007	Z-2324-2008	—	terminated	During setup and potentially during procedures, the breathing bag can become separated from the taped bushing that is part of the breathing bag assembly.
Mar 26, 2004	Z-0892-04	—	terminated	In some cases the device may develop small cracks that could expand over time and result in reduced shelf life or other failure.
Mar 26, 2004	Z-0893-04	—	terminated	In some cases the device may develop small cracks that could expand over time and result in reduced shelf life or other failure.
Mar 26, 2004	Z-0891-04	—	terminated	In some cases the device may develop small cracks that could expand over time and result in reduced shelf life or other failure.
Mar 26, 2004	Z-0894-04	—	terminated	In some cases the device may develop small cracks that could expand over time and result in reduced shelf life or other failure.
Mar 26, 2004	Z-0895-04	—	terminated	In some cases the device may develop small cracks that could expand over time and result in reduced shelf life or other failure.
Apr 15, 2003	Z-0982-03	—	terminated	Printed bag with instructions to verify the pressure with a 'certified manometer' was omitted in some of the product.