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Sign in to claim this brandTRINITY STERILE, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 201 Kiley Dr, SALISBURY, MD, 21801
- Website
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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
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- FDA FEI Number
- 1000123297
- DUNS Number
- —
Catalogue (390)
Page 2 of 8| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Trinity Sterile, Inc. | T97-742 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 1606 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T98-236 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6016 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5019 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81229A | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50508 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 81667 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 10082 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81435 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7039 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50196 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 5034 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5040 | FDA UDI | N/A | Active |
| Trinity Sterile, Inc. | 81359 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 1200XL | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 85286BWMC2 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | T97-776 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5060 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5053 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 85383 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7140 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7209 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81217 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T97-847 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81427 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50186 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 5075 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 1200SM | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T98-496 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 20200 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 10085 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6048 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50881 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 50235 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 50567 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 920306LAC | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50399 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | T97-705 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7219 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7051 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5045 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 20103 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 50907 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 80360 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6006 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 10050 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 85286BWMC | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 7128 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T98-239 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
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Authorities
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FDA Recalls (10)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Dec 13, 2024 | Z-1012-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1016-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1015-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1013-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1014-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Jun 29, 2022 | Z-1551-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Jun 29, 2022 | Z-1548-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Jun 29, 2022 | Z-1550-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Jun 29, 2022 | Z-1549-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Feb 23, 2021 | Z-1468-2021 | — | terminated | Evidence of face masks or other material in the seal in several kits, causing improper seals and compromised sterility |