Seamed Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 18
What Seamed Corp. makes
Seamed Corp. manufactures cardiac pacing system analyzers and diagnostic devices, including standalone units like the SEA MED DDD PACING SYSTEM ANALYZER and multi-channel analyzers such as the SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY. Their portfolio also includes specialized models like the TELECTRONICS MODEL 2401 and the CHRONOCOR VI MODEL 5012, designed for evaluating pacemaker function and signal integrity.
These devices are classified under Class II by the FDA and are listed in the 510(k) registry, indicating they are subject to premarket notification requirements. The company operates from the United States, where its products are regulated under U.S. medical device laws.
Catalogue
Search and filter all 18 devicesFrequently asked questions
How many devices does Seamed Corp. have in the registry?
The registry currently lists 18 devices for Seamed Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seamed Corp.'s devices?
Among its 18 most recently registered devices, Seamed Corp. has devices listed in FDA 510(k) (18 devices).
What risk classes do Seamed Corp.'s devices fall under?
Among its 18 most recently registered devices, the classes recorded for Seamed Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Seamed Corp. in the registry?
The most recently registered devices listed for Seamed Corp. include SEA MED DDD PACING SYSTEM ANALYZER, TELECTRONICS MODEL 2401, SEAMED 4000 and SEAMED MODEL 3200.