Woundchek Laboratories Holdings, Inc. (specification developer, Fall River, MA): 1 new FDA device listing, incl. assay for detection of proteases in chronic wounds
Woundchek Laboratories Holdings, Inc. (Fall River, Massachusetts): 1 new FDA device listing, incl. assay for detection of proteases in chronic wounds. Its amount of 1 is above the median of 2 (50th percentile). Dated 149 days ago, it serves as a historical benchmark. Score 70/100. As of 2026-11-04, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 1 · 50th percentile of 2,709 DeviceEstablishmentPulse records · 0.5x the median
Free preview: all 14 published fields of this record are shown below. Locked: 72 related MA DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Woundchek Laboratories Holdings, Inc. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Fall River, MA, US |
| New listings | 1 |
| Devices | Assay For Detection Of Proteases In Chronic Wounds |
| Product codes | QFA |
| Device classes | Class II |
| Medical specialties | Microbiology |
| Brand names | Woundchek Bacterial Status |
| First new listing | 2026-06-09 |
| Latest new listing | 2026-06-09 |
| FDA registration number | 3011670911 |
| Registration expires | 2027-12-31 |
| amount percentile | 50th of 2,709 (median 2, 0.5x median) |
| Peer records CSV (73 MA records) | 🔒 Click to unlock → |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-06-09
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 21:52:36 GMT
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Peer benchmark and outreach value: Woundchek Laboratories Holdings, Inc. and 73 Massachusetts peers
- Massachusetts DeviceEstablishmentPulse records like this one: 73
- Woundchek Laboratories Holdings, Inc.'s amount: 50th percentile of 2,709 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Massachusetts peer: $14,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
70 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for Woundchek Laboratories Holdings, Inc. in Fall River, Massachusetts?
Woundchek Laboratories Holdings, Inc. (Fall River, MA), a specification developer (outsources manufacturing), added 1 FDA device listing on 2026-06-09.
How does Woundchek Laboratories Holdings, Inc. compare to other Massachusetts DeviceEstablishmentPulse records?
Its amount of 1 sits in the upper half (50th percentile) of 2,709 records; the median is 2. It is 149 days old; check the official source for later updates before acting. Its Score of 70/100 puts it among the stronger signals in this feed.
Woundchek Laboratories Holdings, Inc. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Woundchek Laboratories Holdings, Inc. | Fall River, MA | 1 | 50th | 2026-06-09 |
| Centinel Spine, LLC | West Chester, PA | 3 | 77th | 2026-10-22 |
| TORNIER Inc. | Columbia City, IN | 3 | 77th | 2026-10-21 |
| Davol Inc., Sub. C.R. Bard, Inc. | Warwick, RI | 3 | 77th | 2026-10-14 |
Related records
DeviceEstablishmentPulse: Specification developer (outsources manufacturing) DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Massachusetts
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From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.