Boss Instruments, Ltd.
United Statesfrom the FDA registration address FDA FEI 1000140363
Boss Instruments, Ltd. is a medical device manufacturer, with 9,546 devices listed and 1 FDA recall as of 13 Nov 2026.
- Devices
- 9,546
- Registrations
- FDA
- FDA recalls
- 1
Registry facts
- Registries
- FDA GUDID 3,000
- Device classes
- FDA Class I 2,066
- FDA Class II 934
- FDA recalls
- Identifiers
- FDA FEI 1000140363
At a glance
Market reach
- United States
- FDA FEI, FDA recalls
What Boss Instruments, Ltd. makes
Boss Instruments, Ltd. manufactures reusable surgical instruments, including spinal rongeurs, hand-held retractors, retraction system blades, scissors-like and tweezers-like forceps, general-purpose surgical scissors, needle holders, and bulldog clamps. These tools are designed for soft-tissue manipulation, retraction, and suturing in surgical procedures.
The company’s products are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
Search and filter all 9,546 devicesShowing 1-50 of 9,546
Company details
- FDA FEI number
- 1000140363
- Address
- 104 Sommerfield Drive, Gordonsville, VA, 22942
- Website
- bossinstruments.com/
- facebook.com/bossinstruments
FDA recalls
FDA recall records list 1 recall initiated by Boss Instruments, Ltd., initiated on 2020-06-26. By recorded status: 1 terminated. The reasons filed fall into these groups: mechanical integrity. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 0
- 2020 1
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2020
- 26 Jun 2020 Z-2767-2020 Class II Terminated The tungsten carbide plate, which is intended to hold the sewing needle securely, can break when holding the sewing needle under pressure.
Full distribution text
- 26 Jun 2020 Z-2767-2020 Class II Terminated The tungsten carbide plate, which is intended to hold the sewing needle securely, can break when holding the sewing needle under pressure.
From the company website
BOSS provides the highest quality, German-made surgical instruments and retractor systems, backed by our lifetime guarantee and 30-day easy return policy.
Frequently asked questions
How many devices does Boss Instruments, Ltd. have in the registry?
The registry currently lists 9546 devices for Boss Instruments, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Boss Instruments, Ltd.'s devices?
Among its 50 most recently registered devices, Boss Instruments, Ltd. has devices listed in FDA GUDID (50 devices).
What risk classes do Boss Instruments, Ltd.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Boss Instruments, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Boss Instruments, Ltd.?
FDA recall records list 1 recall initiated by Boss Instruments, Ltd., the most recent initiated on 26 Jun 2020. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Boss Instruments, Ltd. in the registry?
The most recently registered devices listed for Boss Instruments, Ltd. include BOSS Instruments VSX233, BOSS Instruments VSG511, BOSS Instruments 02-1402 and Stealth Surgical SS1671821.