Skip to content

OBP Medical Corporation

Also registered as Obp Medical

Country not established FDA establishment FEI 3007789561

Devices
1
Registrations
FDA
FDA recalls
11 ongoing

Catalogue1

Newest first, rows 1-1 of 1

Company details

FDA FEI number
3007789561
Address
360 MERRIMACK STREET, Lawrence, MA, 01843

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

Recalls initiated per year

  • 2017 0
  • 2018 0
  • 2019 0
  • 2020 0
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 0
  • 2026 1
  • 2026

    • 13 Jul 2026 Z-2933-2026 Class II Ongoing There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient and the healthcare provider. Distribution: Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY,…
      Full distribution text Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, WV and the countries of HKG, CAN, NOR, UAE.
      Submission number: K091937

Frequently asked questions

How many devices does OBP Medical Corporation have in the registry?

The registry currently lists 1 device for OBP Medical Corporation. Devices recorded under merged duplicate company entries are counted once.

Which registries list OBP Medical Corporation's devices?

Among its 1 most recently registered device, OBP Medical Corporation has devices listed in FDA 510(k) (1 device).

What risk classes do OBP Medical Corporation's devices fall under?

Among its 1 most recently registered device, the classes recorded for OBP Medical Corporation's devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for OBP Medical Corporation?

FDA recall records list 1 recall initiated by OBP Medical Corporation, the most recent initiated on 2026-07-13. 1 of them is recorded as ongoing. 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 OBP Medical Corporation in the registry?

The most recently registered devices listed for OBP Medical Corporation include OBP SELF SEALING ENDOSCOPIC SEAL WITH LUER LOCK.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company.