# FDA registered blood borne pathogen response kit manufacturers: 3 in 1 country

Updated November 9, 2026.

There are 3 FDA registered manufacturers of blood borne pathogen response kits in 1 country (product code PWP, Class 1, 21 CFR 880.6250). Each row gives the establishment, its city, its FDA registration number, its role, and its 510(k) clearances, PMA approvals and recalls for this device. 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 0 recall events (0 Class I). FDA data exported November 9, 2026.

## The full list

This record is a row of this list. Pay by card with no account. Prices exclude VAT. CSV and Excel files with the columns this page does not show (establishment name, FDA registration number, FEI number, street, city, state and 11 more), which open on your screen as soon as the payment clears and come by email.

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SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the manufacturers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

- Product code: [PWP](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?search=PWP)
- FDA device name: Blood Borne Pathogen Response Kit
- Device class: 1
- Regulation: 880.6250
- Medical specialty: General Hospital

## Manufacturers by country

| Country | Manufacturers |
| --- | --- |
| United States | 3 |

## Manufacturers of blood borne pathogen response kits

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

| Manufacturer | Location | FDA registration | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| [Aero-Med LLC](https://specstream.ai/data/medical-devices/maker/aero-med-llc-3006191977) | East Hartford, CT, United States | 3006191977 | Contract manufacturer, Manufacturer | 0 |  | 0 | 0 | 0 | [api.fda.gov](https://api.fda.gov/device/registrationlisting.json?search=registration.registration_number:%223006191977%22&limit=1) |
| [Cintas Corporation](https://specstream.ai/data/medical-devices/maker/cintas-corporation-1121142) | Middletown, OH, United States | 1121142 | Manufacturer | 0 |  | 0 | 0 | 0 | [api.fda.gov](https://api.fda.gov/device/registrationlisting.json?search=registration.registration_number:%221121142%22&limit=1) |
| [Normed](https://specstream.ai/data/medical-devices/maker/normed-3013226) | Seattle, WA, United States | 3013226 | Manufacturer, Repackager or relabeler | 0 |  | 0 | 0 | 0 | [api.fda.gov](https://api.fda.gov/device/registrationlisting.json?search=registration.registration_number:%223013226%22&limit=1) |

Source: [openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files)](https://open.fda.gov/data/downloads/). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. FDA registration lists an establishment with the FDA and is not an approval of it: a 510(k) clearance or a PMA approval is for one device.

Free to reuse with credit to SpecStream under [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/).