Threadstone LLC
United StatesFDA applicant, unverified FDA FEI 3017499940
Threadstone LLC is a medical device manufacturer, with 157 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 12 Nov 2026.
- Devices
- 157
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 152
- FDA 510(k) 5
- Device classes
- FDA Class II 157
- Identifiers
- FDA FEI 3017499940
- DUNS 104319989
At a glance
Market reach
- United States
- FDA FEI
What Threadstone LLC makes
Threadstone LLC manufactures polyolefin/fluoropolymer sutures, specifically the HyperSuture product, which is a multifilament suture used for surgical procedures.
The company's devices are classified as Class II and are listed in the FDA 510(k) and FDA UDI registries.
Catalogue
Search and filter all 157 devicesShowing 1-50 of 157
Company details
- FDA FEI number
- 3017499940
- DUNS number
- 104319989
- Address
- 1035 Benfield Blvd Ste H, Millersville, MD, 21108
- Phone
- 4436886483
Frequently asked questions
How many devices does Threadstone LLC have in the registry?
The registry currently lists 157 devices for Threadstone LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Threadstone LLC's devices?
Among its 50 most recently registered devices, Threadstone LLC has devices listed in FDA GUDID (50 devices).
What risk classes do Threadstone LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Threadstone LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Threadstone LLC in the registry?
The most recently registered devices listed for Threadstone LLC include InSet Subscap Repair Kit 2S5KS10011, HyperSuture TST-154L, HyperSuture TST-156L and HyperSuture TSS-504CNL.