# Ventlab Corp.

- Location (FDA's records): Mocksville, NC
- FDA decisions: 23 (1989–2018): 23 510(k) clearances
- Names in FDA's records: Ventlab Corp. (22); Ventlab, LLC (1)
- Product codes: BTM (2), CCK (2), CAF (2), NHK (2), BZO (2), BSJ (1), CBH (1), CAH (1), CAN (1), CAP (1), BTR (1), BTT (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 22 (12 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Mercury Medical: 1 (https://510kreport.com/company/mercury-medical)

## Firms that cite its devices most
- Hsiner Co., Ltd.: 1 (https://510kreport.com/company/hsiner)

## Its most-cited devices
- K012842: V*Care Manual Resuscitator (2001), cited by 1

## Recent decisions
- K173373: SafeT T-Piece Resuscitator (Nov 16, 2018)
- K120118: Ventlab Pressurechek Disosable Column Manometer (May 24, 2012)
- K102674: Cuff Sentry (Jul 22, 2011)
- K093617: Ventlab 6000 Series Humidifier (Jan 27, 2011)
- K093525: Ace/Statcheck II CO2 Indicator, Ace/Statcheck II CO2 Indicator Arm Assemby Adult Statcheck Resuscitator with Ace/Statche (Dec 10, 2009)
- K090840: Ventlab 5000 Series Nebulizer Assembly, Cup, Cup W/ Mask, Cup W/ Fitsall Conn. (Jun 25, 2009)
- K082204: Series SY Disposable Electrosurgical Pad (Aug 13, 2008)
- K063813: Ventlab Nasal CO2 Sampling/O2 Delivery Cannula (Mar 26, 2008)

Source page: https://510kreport.com/company/ventlab