Home › SONTEC INSTRUMENTS, INC. › Battery
Battery
SONTEC INSTRUMENTS, INC. · Model 100-5502 · UDI-DI 00192896112124
HPP
Prescription
0
510(k) clearances
12
Adverse events
1
Recalls
71
Facilities
Description
Battery Only for #100-5500
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-06-11 | Integra LifeSciences Corp. | LED battery chargers may prematurely fail and will not charge the LED battery as intended |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
