FDA.reportPublic FDA data

Lucerno Dynamics, LLC

Matched from indexed company URL: LUCERNO DYNAMICS, LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30129701553012970155Lucerno Dynamics, LLC1N2026-01-01142 Towerview Ct Cary NC US 27513

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00850014578008Lara Reader - B919-371-6800info@lucerno.com
00850014578015Lara Sensor, Type 1 - D919-371-6800info@lucerno.com
00850014578022Lara Sensor, Type 2 - D919-371-6800info@lucerno.com
00850014578039Lara Sensor, Type 3 - D919-371-6800info@lucerno.com
00850014578046Lara Sensor, Type 4 - D919-371-6800info@lucerno.com
00850014578053Lara Sensor, Type 5 - D919-371-6800info@lucerno.com
00850014578060Lara Sensor, Type 6 - D919-371-6800info@lucerno.com
00850014578077Lara Sensor, Type 7 - D919-371-6800info@lucerno.com

Registered Device Listings#

Registration key, Listing key table
Registration keyListing key
1990671565139575
1990671838554191

GUDID#

Sensor Pad - Sensor Pads are intended for use with Lucerno Dynamics sensors on clean, dry, intact skin. The sensor side adhesive is not intended for skin contact. Factors that may impact pad performance include lotion or other skin products, patient movement, and substantial body hair.Sensor Pads consist of a double-coated, two-in-one medical grade silicone adhesive and acrylic tape. The silicone adhesive is hypoallergenic and atraumatic upon removal; it is intended for attachment to the skin. The acrylic tape is intended for attachment to the plastic case of the sensor.

LUCERNO DYNAMICS, LLC

2021-09-22