Seirin-America, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Seirin-America, Inc. makes
Seirin-America, Inc. manufactures acupuncture needles, including intradermal, JR, and Pyonex models.
The company is based in the United States, and its products are regulated as Class II medical devices listed under FDA 510(k) clearances.
Catalogue
Seirin Acupuncture Needles Ref K962809
Regimes: 510(k) Registry: 510(k)Seirin Spinex Intradermal Acupuncture Needles Ref K963769
Regimes: 510(k) Registry: 510(k)Seirin Jr Acupuncture Needles Ref K970260
Regimes: 510(k) Registry: 510(k)Seirin Pyonex Acupuncture Needles Ref K970254
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seirin-America, Inc. have in the registry?
The registry currently lists 4 devices for Seirin-America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seirin-America, Inc.'s devices?
Among its 4 most recently registered devices, Seirin-America, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Seirin-America, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Seirin-America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Seirin-America, Inc. in the registry?
The most recently registered devices listed for Seirin-America, Inc. include SEIRIN ACUPUNCTURE NEEDLES, SEIRIN SPINEX INTRADERMAL ACUPUNCTURE NEEDLES, SEIRIN JR ACUPUNCTURE NEEDLES and SEIRIN PYONEX ACUPUNCTURE NEEDLES.