Data / Medical devices / United States / Thayer Medical Corportation
Thayer Medical Corportation: FDA-registered device maker in Tucson, AZ, United States, 8 510(k) clearances
Thayer Medical Corportation is registered with the FDA (registration 2026894) in Tucson, AZ, United States. It lists 4 device types. The FDA files 8 510(k) clearances under its listings, the newest dated April 1, 2022. 2 recall events name it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2026894
- Address
- 4575 S Palo Verde RD Ste 337, Tucson, AZ, United States, 85714
- Owner or operator
- THAYER MEDICAL CORP. (2026894)
- Roles
- Manufacturer
- First device listed
- October 11, 2007
- Registered through
- 2026
- Brand names listed
- 1008, 1009, 1024, 1024A, 1025, 1025A, 1085, 1088 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Holding Chambers, Direct Patient Interface | NVP | 2 | Manufacturer | accessdata.fda.gov |
| Nebulizer (Direct Patient Interface) | CAF | 2 | Manufacturer | accessdata.fda.gov |
| Percussor, Powered-Electric | BYI | 2 | Manufacturer | accessdata.fda.gov |
| Set, Tubing And Support, Ventilator (W Harness) | BZO | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 1, 2022 | K210558 | LiteAire Basic Dual-Valved, Collapsible MDI Holding Chamber | NVP | Substantially Equivalent | Thayer Medical Corporation | accessdata.fda.gov |
| May 19, 2017 | K160109 | Thayer Medical LiteAire Dual-valved, Collapsible MDI Holding Chamber | NVP | Substantially Equivalent | Thayer Medical Corporation | accessdata.fda.gov |
| September 29, 2011 | K111570 | MINISPACER(R) MDI ADAPTER WITH COUNTER INCREMENTING ACTUATOR | CAF | Substantially Equivalent | Thayer Medical Corporation | accessdata.fda.gov |
| December 10, 2010 | K102658 | MINISPACER DUAL-SPRAY MDI ADAPTER WITH 22MM (OR 15MM) OD / 22MM OD/ID CONNECTIONS / 15MM ID CONNECTIONS | CAF | Substantially Equivalent | Thayer Medical Corp. | accessdata.fda.gov |
| October 26, 2000 | K993101 | LITEAIRE | CAF | Substantially Equivalent | Thayer Medical Corp. | accessdata.fda.gov |
| November 10, 1999 | K992722 | PRIMEAIRE | CAF | Substantially Equivalent | Thayer Medical Corp. | accessdata.fda.gov |
| August 6, 1998 | K974849 | X-AIR-CISER | BYI | Substantially Equivalent | Hougen Mfg., Inc. | accessdata.fda.gov |
| July 18, 1988 | K882341 | QUICK CONNECT T ADAPTOR | BZO | Substantially Equivalent | Thayer Medical Corp. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| September 29, 2016 | 75338 | Class II | Terminated | Thayer MiniSpacer Dual Spray MDI Adapter Counter Incrementing Actuator with 15mm O.D./I.D. Connections, Reference no. 1543A. The 15 mm Dual Spray MiniSpacer with Counter Incrementing Actuator is a non-sterile, single-use | The insert and case label description of the device incorrectly reads Counter Incrementing Actuator with 22mm O.D./I.D. Connections. | accessdata.fda.gov |
| June 6, 2012 | 62283 | Class II | Terminated | AirLife MiniSpacer MDI Dispenser Adapter. Dual-Spray MiniSpacer Metered Dose Inhaler (MDI) Dispenser/Adapter with 15 mm connections. The 15 mm Dual Spray MiniSpacer is a Metered Dose Inhaler (MDI) Dispenser. It is a non- | 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. | accessdata.fda.gov |
Compare with other makers
- All makers of Nebulizer (Direct Patient Interface)
- All makers of Holding Chambers, Direct Patient Interface
- All makers of Set, Tubing And Support, Ventilator (W Harness)
- All makers of Percussor, Powered-Electric
Updated April 1, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.