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THAYER MEDICAL CORPORATION

United States·US-MF-000026197

Last updated May 27, 2026

Information

Country
United States
Address
—
LinkedIn
—
Facebook
—
Phone
1-800-250-3330
PRRC Contact
James Strickland
EUDAMED SRN
US-MF-000026197
FDA FEI Number
—
DUNS Number
626238844

Catalogue (35)

DeviceModel / ReferenceRegistriesClassStatus
Dual Spray Minispacer K955805
FDA 510(k)
Class IIActive
Single Spray Mdi Adapter 1021
FDA UDI
Class IActive
Medline Valved Tee Adapter HCSA1009
FDA UDI
Class IActive
Single Spray Mdi Adapter 1020
FDA UDI
Class IActive
Teleflex Minispacer 1759
FDA UDI
Class IIActive
Medline Valved Tee Adapter HCSA1008
FDA UDI
Class IActive
Quake 1297
FDA UDI
Class IIActive
Valved Tee 1008
EUDAMEDFDA UDI
Class IIaActive
Thayer Hand Held M.k.i. Holding Chamber K924535
FDA 510(k)
Class IIActive
Minispacer Dual-Spray Mdi Adapter With 22mm (or 15mm) Od / 22mm Od/Id Connections / 15mm Id Connections K102658
FDA 510(k)
Class IIActive
LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber K210558
FDA 510(k)
Class IIActive
Thayer Metered Dose Inhaler Dispenser/Adapter K901739
FDA 510(k)
Class IActive
Quick Connect T Adaptor K882341
FDA 510(k)
Class IActive
MiniSpacer® 1024, 1025, 1543 and 1024A, 1025A, 1543A Dual Spray MDI Adapter K233553
FDA 510(k)
Class IIActive
Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber K160109
EUDAMEDFDA 510(k)FDA UDI
Class IIActive
Thayer Suction Evacuation Condensate Collection K900047
FDA 510(k)
Class IActive
Thayer Flexible Condensate Collection System K885088
FDA 510(k)
Class IActive
Thayer Semi-Rigid Condensate Collection System K897057
FDA 510(k)
Class IActive
Thayer Expansion Chamber Metered Dose Inhaler K914283
FDA 510(k)
Class IIActive
Minispacer(r) Mdi Adapter With Counter Incrementing Actuator K111570
FDA 510(k)
Class IIActive
Thayer Semi-Rigid Condensate Collection System K895479
FDA 510(k)
Class IActive
Hand Held Medispacer K972237
FDA 510(k)
Class IIActive
Thayer Mip Adapter K904917
FDA 510(k)
Class IIActive
Thayer Mask To Mouthpiece Adapter/Connector K941026
FDA 510(k)
Class IActive
Valved Tee 1088
EUDAMEDFDA UDI
Class IIaActive
Counter Incrementing Dual Spray MiniSpacer 1024A
EUDAMEDFDA UDI
Class IIaActive
Counter Incrementing Dual Spray MiniSpacer 1025A
EUDAMEDFDA UDI
Class IIaActive
LiteAire BASIC 1803
EUDAMEDFDA UDI
Class IActive
PrimeAire 1114
EUDAMEDFDA UDI
Class IActive
Counter Incrementing Dual Spray MiniSpacer 1543A
EUDAMEDFDA UDI
Class IIaActive
Valved Tee 1009
EUDAMEDFDA UDI
Class IIaActive
LiteAire 1303
EUDAMEDFDA UDI
Class IActive
Dual Spray MiniSpacer 1025
EUDAMEDFDA UDI
Class IIaActive
Dual Spray MiniSpacer 1024
EUDAMEDFDA UDI
Class IIaActive
Valved Tee 1085
EUDAMEDFDA UDI
Class IIaActive

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Notified Bodies

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Authorities

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FDA Recalls (2)

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
Sep 29, 2016Z-1146-2017—terminated

The insert and case label description of the device incorrectly reads Counter Incrementing Actuator with 22mm O.D./I.D. Connections.

Jun 6, 2012Z-1927-2012—terminated

Internal data identified a molding defect in the 15 mm O.D. / I.D. MiniSpacer meter dose inhaler (MDI) adapter that results in an incomplete fill of the aerosol dispensing pathway.